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FDA Inspection
•BAYER PHARMA, AG•June 6, 2024

BAYER PHARMA, AG – FDA Inspection, Jun 6, 2024

Record Details

This FDA Inspection record concerns BAYER PHARMA, AG, with an inspection on June 6, 2024, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
BAYER PHARMA, AG
Inspection Date
June 6, 2024
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • MRA MunizN (Issuing Officer)
View Company Profile

ID · 1d238dca-b4e7-4c8f-8c8c-40de3cf1da86

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1282736
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of BAYER PHARMA, AG

9
DateClassificationOfficeProject area
August 27, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 24, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 3, 2017Not classifiedOffice of Inspections and Investigations
January 24, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 13, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 9 other inspections on the company page
Other documents for BAYER PHARMA, AG
  • FDA Inspection 1239178 - 2021-08-27
  • FDA Inspection 1102816 - 2019-09-24
  • FDA Inspection 1023408 - 2017-07-03
  • FDA Inspection 1001127 - 2017-01-24
  • FDA Inspection 889209 - 2014-05-13

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