FDA Inspection
Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) – FDA Inspection, Feb 9, 2018
Record Details
This FDA Inspection record concerns Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen), with an inspection on February 9, 2018, issued by the Office of Inspections and Investigations, covering human drugs.
- Inspection Date
- February 9, 2018
- Product Type
- Human Drugs
View Company Profile
ID · 7573ddd1-0fbf-4231-a6dc-88dfab638aaa
Inspection Facts
- Inspection number
- 1045220
- FDA center
- Human Drugs
- 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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