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{{#Wiki_filter:NRC FORM 591 M PART 1 | {{#Wiki_filter:NRC FORM 591 M PART 1 U.S. NUCLEAR REGULATORY COMMISSION | ||
\\C. 2012) | |||
*10 CFR 2.201 SAFETY INSPECTION REPORT AND COMPLIANCE INSPECTION 1. LICENSEE/LOCATION INSPECTED: | |||
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REPORT NUMBER(S) l O / 8° 0 0 \\ | |||
REPORT NUMBER(S) l O/ 8° 0 0 \ | 3. DOCKET NUMBER(S) | ||
3. DOCKET NUMBER(S) | 4. LICENSE NUMBER(S) | ||
The inspection was an examination of the activities conducted under your license as they relate to radiation safety and to compliance with the Nuclear Regulatory Commission (NRC) rules and regulations and the conditions of your license. The inspection consisted of selective examinations of procedures and representative records, interviews with personnel, and observations by the inspector. The inspection findings are as follows: | 5. DATE(S) OF INSPECTION I 3-t707J-t} 1 t1/Jo/1i LICENSEE: | ||
The inspection was an examination of the activities conducted under your license as they relate to radiation safety and to compliance with the Nuclear Regulatory Commission (NRC) rules and regulations and the conditions of your license. The inspection consisted of selective examinations of procedures and representative records, interviews with personnel, and observations by the inspector. The inspection findings are as follows: | |||
[!{' Based on the inspection findings, no violations were identifie. | |||
Statement of Corrective Actions I hereby state that, within 30 days, the actions described by me to the Inspector will be taken to correct the violations identified. This statement of corrective actions is made in accordance with the requirements of 10 CFR 2.201 (corrective steps already taken, corrective steps which will be taken, date when full compliance will be achieved). I understand that no further written response to NRC will be required, unless specifically requeste TITLE | D D Previous violation(s) close The violations(s), specifically described to you by the inspector as non-cited violations, are not being cited because they were self-identified, non-repetitive, and corrective action was or is being taken, and the remaining criteria in the NRC Enforcement Policy, to exercise discretion, were satisfie Non-cited violation{s) were discussed involving the following requirement(s): | ||
NRC FORM 591M PART 1 (07-2012) | During this inspection, certain of your activities, as described below and/or attached, were in violation of NRC requirements and are being cited in accordance with NRC Enforcement Policy. This form is a NOTICE OF VIOLATION, which may be subject to posting in accordance with 10 CFR 19.1 (Violations and Corrective Actions) | ||
Statement of Corrective Actions I hereby state that, within 30 days, the actions described by me to the Inspector will be taken to correct the violations identified. This statement of corrective actions is made in accordance with the requirements of 10 CFR 2.201 (corrective steps already taken, corrective steps which will be taken, date when full compliance will be achieved). I understand that no further written response to NRC will be required, unless specifically requeste TITLE PRINTED NAME SIGNATURE DATE LICENSEE'S REPRESENTATIVE NRC INSPECTOR BRANCH CHIEF NRC FORM 591M PART 1 (07-2012) | |||
I | |||
NRC FORM 591 M PART 3 | NRC FORM 591 M PART 3 (07-2012) | ||
10 CFR 2.201 Docket File Information SAFETY INSPECTION REPORT AND COMPLIANCE INSPECTION 1. LICENSEE/LOCATION INSPECTED: | 10 CFR 2.201 U.S. NUCLEAR REGULA TORY COMMISSION Docket File Information SAFETY INSPECTION REPORT AND COMPLIANCE INSPECTION 1. LICENSEE/LOCATION INSPECTED: | ||
Porter Regional Hospital 85 E. U.S. Highway 6 Valparaiso, IN REPORT NUMBER(S} 2018001 3. DOCKET NUMBER(S) | |||
030-12150 6. INSPECTION PROCEDURES USED 87132 2. NRG/REGIONAL OFFICE 4. LICENSE NUMBER(S) | |||
13-17073-01 Region III U.S. Nuclear Regulatory Commission 2443 Warrenville Road, Suite 210 Lisle, IL 60532-4352 5. DATE(S) OF INSPECTION 11/30/18 7. INSPECTION FOCUS AREAS 02.01, 02.02, 02.04, 02.05, 02.06, 02.07, 02.09 SUPPLEMENTAL INSPECTION INFORMATION 1. PROGRAM CODE(S) | |||
02240 2. PRIORITY | |||
[lJ Main Office Inspection D Field Office Inspection D Temporary Job Site Inspection 3. LICENSEE CONTACT James Forde, M.D., RSO Next Inspection Date: | |||
PROGRAM SCOPE 4. TELEPHONE NUMBER (219) 983-8300 11/30/2020 This was an unannounced, routine inspection. The licensee had a 300-bed main hospital located in Valparaiso, Indiana, authorized for materials and uses permitted by 35.100, 35.200, 35.300, 35.400, and 35.1000 (yttrium-90 SIR-Spheres); a cardiology center in Valparaiso, Indiana, authorized for uses of 35.100 and 35.200 materials; and a PET Center in Chesterton, Indiana authorized for uses of 35.100 and 35.200 materials. That PET Center is planned to be decommissioned. The new PET Center will be located at the main hospital. The licensee employed 7 full-time nuclear medicine technologists (NMTs), and with the exception of 1 NMT dedicated to the cardiology center, provided coverage at all three locations on a rotational basis. Approximately 425 diagnostic nuclear medicine procedures were performed monthly at the main hospital; approximately 200 diagnostic nuclear medicine procedures (cardiology only) | |||
were performed monthly at the cardiology center, and approximately 50 procedures using F-18 (FOG) were performed monthly at the PET center. The licensee (main hospital only) performed approximately two administrations of sodium iodide 1-131 per month (whole body scan, thyroid cancer treatment, and hyperthyroid treatment). The licensee last administered Ra-223 dichloride (Xofigo) on 10/4/17. The licensee performed several Y-90 SIR-Spheres treatments. The licensee had not conducted 35.400 treatments since about 201 Performance Observations The inspector: ( 1) toured the new PET Center at the main hospital that was in the. construction phase, and noted that the layout was as per the facility diagram in the licensee's letter dated 6/12/18; (2) noted that there were no therapies during the inspection; (3) observed licensed material secured and posted as required; (4) observed a nuclear medicine technologist (NMT) prepare a technetium-99m Cardiolite dosage for a cardiac stress imaging test using proper radiation safety techniques; (5) noted that the licensee's survey instruments were calibrated; (6) reviewed selected records of yttrium-90 SIR-Spheres treatments, including liver to lung shunt tests prior to yttrium-90 SIR-Spheres administration; (7) | were performed monthly at the cardiology center, and approximately 50 procedures using F-18 (FOG) were performed monthly at the PET center. The licensee (main hospital only) performed approximately two administrations of sodium iodide 1-131 per month (whole body scan, thyroid cancer treatment, and hyperthyroid treatment). The licensee last administered Ra-223 dichloride (Xofigo) on 10/4/17. The licensee performed several Y-90 SIR-Spheres treatments. The licensee had not conducted 35.400 treatments since about 201 Performance Observations The inspector: ( 1) toured the new PET Center at the main hospital that was in the. construction phase, and noted that the layout was as per the facility diagram in the licensee's letter dated 6/12/18; (2) noted that there were no therapies during the inspection; (3) observed licensed material secured and posted as required; (4) observed a nuclear medicine technologist (NMT) prepare a technetium-99m Cardiolite dosage for a cardiac stress imaging test using proper radiation safety techniques; (5) noted that the licensee's survey instruments were calibrated; (6) reviewed selected records of yttrium-90 SIR-Spheres treatments, including liver to lung shunt tests prior to yttrium-90 SIR-Spheres administration; (7) | ||
reviewed dosimeter records since the last inspection to date, and the highest annual doses of whole body and extremity were 244 millirem (mrem) and 950 mrem, respectively; and (8) reviewed selected records of iodine-131 use and a Xofigo treatment in 201 No violations ofNRC regulatory requirements were identified as a result of this | reviewed dosimeter records since the last inspection to date, and the highest annual doses of whole body and extremity were 244 millirem (mrem) and 950 mrem, respectively; and (8) reviewed selected records of iodine-131 use and a Xofigo treatment in 201 No violations ofNRC regulatory requirements were identified as a result of this inspectio NRC FORM 591M PART 3 (07-2012) | ||
NRC FORM 591M PART 3 (07-2012) | |||
}} | }} | ||
Latest revision as of 08:20, 5 January 2025
| ML18348A755 | |
| Person / Time | |
|---|---|
| Site: | 03012150, 015000201 |
| Issue date: | 11/30/2018 |
| From: | Gattone R NRC/RGN-III |
| To: | Forde J Porter Regional Hospital |
| References | |
| IR 2018001 | |
| Download: ML18348A755 (2) | |
Text
NRC FORM 591 M PART 1 U.S. NUCLEAR REGULATORY COMMISSION
\\C. 2012)
- 10 CFR 2.201 SAFETY INSPECTION REPORT AND COMPLIANCE INSPECTION 1. LICENSEE/LOCATION INSPECTED:
fort-er ~t9 ;uNrd H.,.rp;t~I 8S f. V, >. Hwy 6 2. NRC/f\\EGIONAL OFFICE Re..,,,,,., +.
- l. yt,J W~f',t,..,w, II~
~ ~-
VD\\ I p~r~;so., I..rl l-i s lc, XL 60S3" Select a location (Use keyboard arrows to select)...
REPORT NUMBER(S) l O / 8° 0 0 \\
3. DOCKET NUMBER(S)
4. LICENSE NUMBER(S)
5. DATE(S) OF INSPECTION I 3-t707J-t} 1 t1/Jo/1i LICENSEE:
The inspection was an examination of the activities conducted under your license as they relate to radiation safety and to compliance with the Nuclear Regulatory Commission (NRC) rules and regulations and the conditions of your license. The inspection consisted of selective examinations of procedures and representative records, interviews with personnel, and observations by the inspector. The inspection findings are as follows:
[!{' Based on the inspection findings, no violations were identifie.
D D Previous violation(s) close The violations(s), specifically described to you by the inspector as non-cited violations, are not being cited because they were self-identified, non-repetitive, and corrective action was or is being taken, and the remaining criteria in the NRC Enforcement Policy, to exercise discretion, were satisfie Non-cited violation{s) were discussed involving the following requirement(s):
During this inspection, certain of your activities, as described below and/or attached, were in violation of NRC requirements and are being cited in accordance with NRC Enforcement Policy. This form is a NOTICE OF VIOLATION, which may be subject to posting in accordance with 10 CFR 19.1 (Violations and Corrective Actions)
Statement of Corrective Actions I hereby state that, within 30 days, the actions described by me to the Inspector will be taken to correct the violations identified. This statement of corrective actions is made in accordance with the requirements of 10 CFR 2.201 (corrective steps already taken, corrective steps which will be taken, date when full compliance will be achieved). I understand that no further written response to NRC will be required, unless specifically requeste TITLE PRINTED NAME SIGNATURE DATE LICENSEE'S REPRESENTATIVE NRC INSPECTOR BRANCH CHIEF NRC FORM 591M PART 1 (07-2012)
I
NRC FORM 591 M PART 3 (07-2012)
10 CFR 2.201 U.S. NUCLEAR REGULA TORY COMMISSION Docket File Information SAFETY INSPECTION REPORT AND COMPLIANCE INSPECTION 1. LICENSEE/LOCATION INSPECTED:
Porter Regional Hospital 85 E. U.S. Highway 6 Valparaiso, IN REPORT NUMBER(S} 2018001 3. DOCKET NUMBER(S)
030-12150 6. INSPECTION PROCEDURES USED 87132 2. NRG/REGIONAL OFFICE 4. LICENSE NUMBER(S)
13-17073-01 Region III U.S. Nuclear Regulatory Commission 2443 Warrenville Road, Suite 210 Lisle, IL 60532-4352 5. DATE(S) OF INSPECTION 11/30/18 7. INSPECTION FOCUS AREAS 02.01, 02.02, 02.04, 02.05, 02.06, 02.07, 02.09 SUPPLEMENTAL INSPECTION INFORMATION 1. PROGRAM CODE(S)
02240 2. PRIORITY
[lJ Main Office Inspection D Field Office Inspection D Temporary Job Site Inspection 3. LICENSEE CONTACT James Forde, M.D., RSO Next Inspection Date:
PROGRAM SCOPE 4. TELEPHONE NUMBER (219) 983-8300 11/30/2020 This was an unannounced, routine inspection. The licensee had a 300-bed main hospital located in Valparaiso, Indiana, authorized for materials and uses permitted by 35.100, 35.200, 35.300, 35.400, and 35.1000 (yttrium-90 SIR-Spheres); a cardiology center in Valparaiso, Indiana, authorized for uses of 35.100 and 35.200 materials; and a PET Center in Chesterton, Indiana authorized for uses of 35.100 and 35.200 materials. That PET Center is planned to be decommissioned. The new PET Center will be located at the main hospital. The licensee employed 7 full-time nuclear medicine technologists (NMTs), and with the exception of 1 NMT dedicated to the cardiology center, provided coverage at all three locations on a rotational basis. Approximately 425 diagnostic nuclear medicine procedures were performed monthly at the main hospital; approximately 200 diagnostic nuclear medicine procedures (cardiology only)
were performed monthly at the cardiology center, and approximately 50 procedures using F-18 (FOG) were performed monthly at the PET center. The licensee (main hospital only) performed approximately two administrations of sodium iodide 1-131 per month (whole body scan, thyroid cancer treatment, and hyperthyroid treatment). The licensee last administered Ra-223 dichloride (Xofigo) on 10/4/17. The licensee performed several Y-90 SIR-Spheres treatments. The licensee had not conducted 35.400 treatments since about 201 Performance Observations The inspector: ( 1) toured the new PET Center at the main hospital that was in the. construction phase, and noted that the layout was as per the facility diagram in the licensee's letter dated 6/12/18; (2) noted that there were no therapies during the inspection; (3) observed licensed material secured and posted as required; (4) observed a nuclear medicine technologist (NMT) prepare a technetium-99m Cardiolite dosage for a cardiac stress imaging test using proper radiation safety techniques; (5) noted that the licensee's survey instruments were calibrated; (6) reviewed selected records of yttrium-90 SIR-Spheres treatments, including liver to lung shunt tests prior to yttrium-90 SIR-Spheres administration; (7)
reviewed dosimeter records since the last inspection to date, and the highest annual doses of whole body and extremity were 244 millirem (mrem) and 950 mrem, respectively; and (8) reviewed selected records of iodine-131 use and a Xofigo treatment in 201 No violations ofNRC regulatory requirements were identified as a result of this inspectio NRC FORM 591M PART 3 (07-2012)