FDA Inspection 1012240 — Excella GmbH & Co. KG

Excella GmbH & Co. KG — FEI 3000242652

The FDA completed an inspection of Excella GmbH & Co. KG on Mar 17, 2017 in Feucht. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Veterinary.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Mar 17, 2017
Fiscal Year
2017
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.