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FDA Inspection 1003153 — Thymoorgan Pharmazie Gmbh

Thymoorgan Pharmazie Gmbh — FEI 3002320821

The FDA completed an inspection of Thymoorgan Pharmazie Gmbh on December 16, 2016 in Goslar. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 16, 2016
Fiscal Year
2017
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))
  • 943847 (NAI Thu Sep 24 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

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