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FDA Inspection
•Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)•July 20, 2020

Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) – FDA Inspection, Jul 20, 2020

Record Details

This FDA Inspection record concerns Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen), with an inspection on July 20, 2020, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)
Inspection Date
July 20, 2020
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 44a48041-c6d9-4edf-89ce-e07238e54fe5

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1155760
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)

12
DateClassificationOfficeProject area
March 19, 2024Not classifiedOffice of Inspections and Investigations
July 21, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 19, 2023NAICenter for Devices and Radiological HealthCompliance: Devices
July 17, 2019Not classifiedOffice of Inspections and Investigations
June 12, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 12 other inspections on the company page
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 1097448 - 2019-07-17
  • FDA Inspection 1060641 - 2018-06-12

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