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FDA Inspection
•Vetter Pharma Fertigung GmbH & Co. KG•May 17, 2019

Vetter Pharma Fertigung GmbH & Co. KG – FDA Inspection, May 17, 2019

Record Details

This FDA Inspection record concerns Vetter Pharma Fertigung GmbH & Co. KG, with an inspection on May 17, 2019, issued by the Office of Inspections and Investigations, covering biologics.

Company
Vetter Pharma Fertigung GmbH & Co. KG
Inspection Date
May 17, 2019
Product Type
Biologics
Office
Office of Inspections and Investigations
People
  • Mizanne E. Lewis (Company Rep)
  • Prabhu P. Raju (FDA Associated Person)
View Company Profile

ID · 7ffc5979-4d41-4da9-a03d-30a38b4c6044

Inspection Facts

Inspection number
1095644
FDA center
Biologics
Outcome
Form 483 issued

Other FDA inspections of Vetter Pharma Fertigung GmbH & Co. KG

12
DateClassificationOfficeProject area
September 20, 2024Not classifiedOffice of Inspections and Investigations
March 17, 2023Not classifiedOffice of Inspections and Investigations
July 13, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 11, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 17, 2017VAICenter 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
  • FDA Inspection 1248795 - 2024-09-20
  • FDA Inspection 1203580 - 2023-03-17
  • FDA Inspection 1241531 - 2022-07-13
  • FDA Inspection 1129698 - 2019-09-11
  • FDA Inspection 1000875 - 2017-01-17

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