FDA Inspection 831974 — Excella GmbH & Co. KG

Excella GmbH & Co. KG — FEI 3000242652

The FDA completed an inspection of Excella GmbH & Co. KG on May 17, 2013 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: Veterinary.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
May 17, 2013
Fiscal Year
2013
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Feucht (Germany)

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