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FDA Inspection
•Vetter Pharma Fertigung GmbH & Co. KG•May 24, 2022

Vetter Pharma Fertigung GmbH & Co. KG – FDA Inspection, May 24, 2022

Record Details

This FDA Inspection record concerns Vetter Pharma Fertigung GmbH & Co. KG, with an inspection on May 24, 2022, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Vetter Pharma Fertigung GmbH & Co. KG
Inspection Date
May 24, 2022
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 715b1b50-164b-48a6-8e18-a8ed33f149b9

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1205983
FDA center
Human Drugs
Project area
Drug Quality Assurance

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

9
DateClassificationOfficeProject area
April 24, 2024Not classifiedOffice of Inspections and Investigations
February 24, 2023Not classifiedOffice of Inspections and Investigations
September 13, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 21, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 10, 2017VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 9 other inspections on the company page
Other documents for Vetter Pharma Fertigung GmbH & Co. KG
  • FDA Inspection 1234265 - 2024-04-24
  • FDA Inspection 1201723 - 2023-02-24
  • FDA Inspection 1129699 - 2019-09-13
  • FDA Inspection 1070717 - 2018-09-21
  • FDA Inspection 1031350 - 2017-11-10

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