FDA Inspection
Centurion Medical Products LPCenturion Medical Products LP – FDA Inspection, Mar 31, 2015
Record Details
This FDA Inspection record concerns Centurion Medical Products LP, with an inspection on March 31, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- March 31, 2015
- Product Type
- Devices
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ID · 5e02fdaa-9fd1-486b-aa76-69b66f6c24b3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 920176
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.25(b)Training - Lack of or inadequate procedures
- 21 CFR 803.17(b)(1)Info evaluated to determine if event was reportable
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Centurion Medical Products LP
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 17, 2018 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 14, 2017 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 16, 2011 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 28, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Centurion Medical Products LP
- FDA Inspection 1079526 - 2018-08-17
- FDA Inspection 1008388 - 2017-02-14
- FDA Inspection 759043 - 2011-12-16
- FDA Inspection 669727 - 2010-06-28
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