Home / Inspections / 778568

FDA Inspection 778568 — Eurofins Lancaster Laboratories, Inc

Eurofins Lancaster Laboratories, Inc — FEI 1833335

The FDA completed an inspection of Eurofins Lancaster Laboratories, Inc on April 25, 2012 in Portage, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Veterinary.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 25, 2012
Fiscal Year
2012
Product Type
Veterinary
Project Area
Pre-Approval Eval. of Animal Drugs and Food Additives
Location
Portage, MI (United States)

Facility

Other inspections at this facility

  • 1272016 (VAI Fri May 30 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1160560 (NAI Fri Dec 10 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1080439 (NAI Wed Jan 23 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1045298 (NAI Fri Feb 23 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1001348 (NAI Fri Nov 04 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources