FDA Inspection
Vipamat SARLVipamat SARL – FDA Inspection, Nov 16, 2017
Record Details
This FDA Inspection record concerns Vipamat SARL, with an inspection on November 16, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
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ID · b1e5b9f4-2abb-46eb-9ea6-eeddb0d964a9
Inspection Facts
- Inspection number
- 1031444
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 820.184DHR - not or inadequately maintained
- 21 CFR 820.184Lack of or inadequate DHR procedures
- 21 CFR 820.22Quality audits - auditor independence
- 21 CFR 820.22Quality Audits - defined intervals
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Other FDA inspections of Vipamat SARL
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 18, 2026 | Not classified | Office of Inspections and Investigations | |
| October 26, 2023 | Not classified | Office of Inspections and Investigations | |
| December 4, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 27, 2011 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Vipamat SARL
- FDA Inspection 1312406 - 2026-03-18
- FDA Inspection 1222659 - 2023-10-26
- FDA Inspection 911564 - 2014-12-04
- FDA Inspection 712630 - 2011-01-27
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