FDA Inspection
Vetter Pharma Fertigung GmbH & Co. KGVetter Pharma Fertigung GmbH & Co. KG – FDA Inspection, Jan 17, 2017
Record Details
This FDA Inspection record concerns Vetter Pharma Fertigung GmbH & Co. KG, with an inspection on January 17, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · b558ef9e-1f16-4247-802d-bdc447e850e3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1000875
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
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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