FDA Inspection 898000 — Almirall Hermal GmbH

Almirall Hermal GmbH — FEI 3002807154

The FDA completed an inspection of Almirall Hermal GmbH on September 26, 2014 in Reinbek. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 26, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Reinbek (Germany)