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FDA Inspection
•BAYER PHARMA, AG•July 3, 2017

BAYER PHARMA, AG – FDA Inspection, Jul 3, 2017

Record Details

This FDA Inspection record concerns BAYER PHARMA, AG, with an inspection on July 3, 2017, issued by the Office of Inspections and Investigations, covering human drugs.

Company
BAYER PHARMA, AG
Inspection Date
July 3, 2017
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Helen B. Ricalde (FDA Associated Person)
View Company Profile

ID · 4cad4b59-7cd0-472e-b6f8-749df0c15721

Inspection Facts

Inspection number
1023408
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of BAYER PHARMA, AG

9
DateClassificationOfficeProject area
June 6, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 27, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 24, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
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 1282736 - 2024-06-06
  • FDA Inspection 1239178 - 2021-08-27
  • FDA Inspection 1102816 - 2019-09-24
  • FDA Inspection 1001127 - 2017-01-24
  • FDA Inspection 889209 - 2014-05-13

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