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FDA Inspection 1116639 — LTS Lohmann Therapie-Systeme AG

LTS Lohmann Therapie-Systeme AG — FEI 3003387535

The FDA completed an inspection of LTS Lohmann Therapie-Systeme AG on October 31, 2019 in Andernach. 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
October 31, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Andernach (Germany)

Additional Details

Mutual Recognition Agreement (MRA)

Facility

Other inspections at this facility

  • 1264907 (NAI Wed May 18 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1025276 (VAI Fri Sep 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 865616 (NAI Fri Dec 20 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 735498 (VAI Tue Jun 21 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 605480 (NAI Thu Jun 18 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources