FDA Inspection 1041324 — Profil Mainz GmbH & Co. KG

Profil Mainz GmbH & Co. KG — FEI 3013981932

The FDA completed an inspection of Profil Mainz GmbH & Co. KG on Jan 16, 2018 in Mainz. 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
Jan 16, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Mainz (Germany)

Additional Details

Clinical BA/BE

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