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FDA Inspection 1080439 — Eurofins Lancaster Laboratories, Inc

Eurofins Lancaster Laboratories, Inc — FEI 1833335

The FDA completed an inspection of Eurofins Lancaster Laboratories, Inc on January 23, 2019 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
January 23, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Portage, MI (United States)

Facility

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FDA data resources