FDA Inspection 735498 — LTS Lohmann Therapie-Systeme AG

LTS Lohmann Therapie-Systeme AG — FEI 3003387535

The FDA completed an inspection of LTS Lohmann Therapie-Systeme AG on Jun 21, 2011 in Andernach. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 21, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Andernach (Germany)

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