FDA Inspection 1205496 — Excella GmbH & Co. KG

Excella GmbH & Co. KG — FEI 3000242652

The FDA completed an inspection of Excella GmbH & Co. KG on Oct 19, 2022 in Feucht. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 19, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Feucht (Germany)

Additional details

Mutual Recognition Agreement (MRA)

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