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FDA Inspection
•Wacker Biotech GmbH•April 11, 2017

Wacker Biotech GmbH – FDA Inspection, Apr 11, 2017

Record Details

This FDA Inspection record concerns Wacker Biotech GmbH, with an inspection on April 11, 2017, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Wacker Biotech GmbH
Inspection Date
April 11, 2017
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Wayne E. Seifert (Senior Regulatory Specialist)
  • Zhihao Pete Qiu (Issuing Officer)
View Company Profile

ID · ae9705c8-b638-400a-959e-838dc1f37a02

Inspection Facts

Inspection number
1006578
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Wacker Biotech GmbH

2
DateClassificationOfficeProject area
December 7, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 6, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Wacker Biotech GmbH
  • FDA Inspection 1288878 - 2023-12-07
  • FDA Inspection 1110441 - 2019-09-06

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