FDA Inspection 1270072 — Almirall Hermal GmbH

Almirall Hermal GmbH — FEI 3002807154

The FDA completed an inspection of Almirall Hermal GmbH on May 6, 2021 in Reinbek. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 6, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Reinbek (Germany)

Additional Details

Mutual Recognition Agreement (MRA)