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FDA Inspection
•Aesica Pharmaceutical GmbH•September 12, 2024

Aesica Pharmaceutical GmbH – FDA Inspection, Sep 12, 2024

Record Details

This FDA Inspection record concerns Aesica Pharmaceutical GmbH, with an inspection on September 12, 2024, covering drugs.

Company
Aesica Pharmaceutical GmbH
Inspection Date
September 12, 2024
Product Type
Drugs
View Company Profile

ID · 50b4ff3b-c8a7-4b8e-8f38-e84917ae532b

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1306304
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Aesica Pharmaceutical GmbH

4
DateClassificationOfficeProject area
July 1, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 20, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 17, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 11, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Aesica Pharmaceutical GmbH
  • FDA Inspection 1190265 - 2021-07-01
  • FDA Inspection 1032046 - 2017-09-20
  • FDA Inspection 866229 - 2014-01-17
  • FDA Inspection 759369 - 2011-11-11

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