FDA Inspection 1251085 — AMRYT GMBH

AMRYT GMBH — FEI 3014849838

The FDA completed an inspection of AMRYT GMBH on December 6, 2022 in Niefern-Oschelbronn. 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
December 6, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Niefern-Oschelbronn (Germany)

Additional Details

Mutual Recognition Agreement (MRA)