FDA Inspection 1001348 — Eurofins Lancaster Laboratories, Inc
The FDA completed an inspection of Eurofins Lancaster Laboratories, Inc on Nov 4, 2016 in Portage, MI. 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
- Nov 4, 2016
- Fiscal Year
- 2017
- Product Type
- Veterinary
- Project Area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
- Location
- Portage, MI (United States)