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FDA Inspection 1160560 — Eurofins Lancaster Laboratories, Inc

Eurofins Lancaster Laboratories, Inc — FEI 1833335

The FDA completed an inspection of Eurofins Lancaster Laboratories, Inc on December 10, 2021 in Portage, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 10, 2021
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
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))
  • 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))
  • 889635 (VAI Fri Aug 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources