FDA Inspection 971695 — Dr. Paul Lohmann GmbH KG

Dr. Paul Lohmann GmbH KG — FEI 3004273210

The FDA completed an inspection of Dr. Paul Lohmann GmbH KG on Apr 14, 2016 in Luneburg. 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
Apr 14, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Luneburg (Germany)

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