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FDA Inspection
•Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)•April 19, 2023

Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) – FDA Inspection, Apr 19, 2023

Record Details

This FDA Inspection record concerns Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen), with an inspection on April 19, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company
Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)
Inspection Date
April 19, 2023
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Shannon A. Gregory (Investigator)
View Company Profile

ID · 60736d3b-56cc-4fc9-9e88-5d6eaeeb65d0

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1205732
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

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
July 20, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
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 1155760 - 2020-07-20
  • FDA Inspection 1097448 - 2019-07-17
  • FDA Inspection 1060641 - 2018-06-12

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