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FDA Inspection 883211 — Thymoorgan Pharmazie Gmbh

Thymoorgan Pharmazie Gmbh — FEI 3002320821

The FDA completed an inspection of Thymoorgan Pharmazie Gmbh on May 22, 2014 in Goslar. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 22, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Goslar (Germany)

Facility

Other inspections at this facility

  • 1203954 (VAI Tue Apr 25 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1207607 (VAI Thu Oct 06 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1123031 (VAI Thu Jun 20 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1053793 (NAI Mon Apr 23 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1003153 (NAI Fri Dec 16 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources