FDA Inspection
Vetter Pharma Fertigung GmbH & Co. KGVetter Pharma Fertigung GmbH & Co. KG – FDA Inspection, Dec 5, 2013
Record Details
This FDA Inspection record concerns Vetter Pharma Fertigung GmbH & Co. KG, with an inspection on December 5, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- December 5, 2013
- Product Type
- Devices
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ID · a29a64fc-2b7f-4a0f-ab35-7a5c0d5f996f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 863242
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of Vetter Pharma Fertigung GmbH & Co. KG
12| Date | Classification | Office | Project area |
|---|---|---|---|
| September 20, 2024 | Not classified | Office of Inspections and Investigations | |
| March 17, 2023 | Not classified | Office of Inspections and Investigations | |
| July 13, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 11, 2019 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 17, 2019 | Not classified | Office of Inspections and Investigations |
Other documents for Vetter Pharma Fertigung GmbH & Co. KG
- FDA Inspection 1248795 - 2024-09-20
- FDA Inspection 1203580 - 2023-03-17
- FDA Inspection 1241531 - 2022-07-13
- FDA Inspection 1129698 - 2019-09-11
- FDA Inspection 1095644 - 2019-05-17
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