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FDA Inspection
•Vetter Pharma Fertigung GmbH & Co. KG•September 20, 2024

Vetter Pharma Fertigung GmbH & Co. KG – FDA Inspection, Sep 20, 2024

Record Details

This FDA Inspection record concerns Vetter Pharma Fertigung GmbH & Co. KG, with an inspection on September 20, 2024, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Vetter Pharma Fertigung GmbH & Co. KG
Inspection Date
September 20, 2024
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Jiangsong Jiang (Issuing Officer)
  • Richard Ledwidge
  • Thuy T. Nguyen (FDA Associated Person)
View Company Profile

ID · 1c303c5b-09c0-49eb-a402-b5c1add5218e

Inspection Facts

Inspection number
1248795
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

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

12
DateClassificationOfficeProject area
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
May 17, 2019Not classifiedOffice of Inspections and Investigations
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 1203580 - 2023-03-17
  • FDA Inspection 1241531 - 2022-07-13
  • FDA Inspection 1129698 - 2019-09-11
  • FDA Inspection 1095644 - 2019-05-17
  • FDA Inspection 1000875 - 2017-01-17

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