FDA Inspection 778568 — Eurofins Lancaster Laboratories, Inc
The FDA completed an inspection of Eurofins Lancaster Laboratories, Inc on Apr 25, 2012 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
- Apr 25, 2012
- Fiscal Year
- 2012
- Product Type
- Veterinary
- Project Area
- Pre-Approval Eval. of Animal Drugs and Food Additives
- Location
- Portage, MI (United States)