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FDA Inspection
•Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)•March 19, 2024

Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) – FDA Inspection, Mar 19, 2024

Record Details

This FDA Inspection record concerns Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen), with an inspection on March 19, 2024, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)
Inspection Date
March 19, 2024
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Bo Chi (Issuing Officer)
  • Leiyun W. Boone (Issuing Officer)
  • Olumide A. Martins (Issuing Officer)
  • Orlando Martins (Issuing Officer)
View Company Profile

ID · f6e95b0e-284c-4500-abbe-da42943240ea

Inspection Facts

Inspection number
1242049
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

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

12
DateClassificationOfficeProject area
July 21, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 19, 2023NAICenter for Devices and Radiological HealthCompliance: Devices
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 1253708 - 2023-07-21
  • FDA Inspection 1205732 - 2023-04-19
  • FDA Inspection 1155760 - 2020-07-20
  • FDA Inspection 1097448 - 2019-07-17
  • FDA Inspection 1060641 - 2018-06-12

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