FDA Inspection 865616 — LTS Lohmann Therapie-Systeme AG

LTS Lohmann Therapie-Systeme AG — FEI 3003387535

The FDA completed an inspection of LTS Lohmann Therapie-Systeme AG on Dec 20, 2013 in Andernach. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Dec 20, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Andernach (Germany)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.