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FDA Inspection
•BIPSO GmbH•November 7, 2019

BIPSO GmbH – FDA Inspection, Nov 7, 2019

Record Details

This FDA Inspection record concerns BIPSO GmbH, with an inspection on November 7, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
BIPSO GmbH
Inspection Date
November 7, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · b560ab0a-05fd-40b3-afec-ca823e7652d9

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1125102
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of BIPSO GmbH

5
DateClassificationOfficeProject area
May 4, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 30, 2018Not classifiedOffice of Inspections and Investigations
June 17, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 11, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 10, 2012NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for BIPSO GmbH
  • FDA Inspection 1278362 - 2022-05-04
  • FDA Inspection 1058876 - 2018-05-30
  • FDA Inspection 986231 - 2016-06-17
  • FDA Inspection 868627 - 2014-02-11
  • FDA Inspection 784924 - 2012-05-10

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