FDA Inspection
Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) – FDA Inspection, Nov 2, 2017
Record Details
This FDA Inspection record concerns Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen), with an inspection on November 2, 2017, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- November 2, 2017
- Product Type
- Biologics
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ID · eb2b0232-ce70-42ae-a80c-78a34a6556e8
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1031348
- FDA center
- Biologics
- Project area
- Blood and Blood Products
- Outcome
- Form 483 issued
Other FDA inspections of Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)
12| Date | Classification | Office | Project area |
|---|---|---|---|
| March 19, 2024 | Not classified | Office of Inspections and Investigations | |
| July 21, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 19, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 20, 2020 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 17, 2019 | Not classified | Office of Inspections and Investigations |
Other documents for Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)
- FDA Inspection 1242049 - 2024-03-19
- FDA Inspection 1253708 - 2023-07-21
- FDA Inspection 1205732 - 2023-04-19
- FDA Inspection 1155760 - 2020-07-20
- FDA Inspection 1097448 - 2019-07-17
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