FDA Inspection 1205496 — Excella GmbH & Co. KG

Excella GmbH & Co. KG — FEI 3000242652

The FDA completed an inspection of Excella GmbH & Co. KG on October 19, 2022 in Feucht. 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
October 19, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Feucht (Germany)

Additional Details

Mutual Recognition Agreement (MRA)