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FDA Inspection 983488 — Eurofins Viracor, LLC.

Eurofins Viracor, LLC. — FEI 3005651716

The FDA completed an inspection of Eurofins Viracor, LLC. on September 2, 2016 in Lenexa, KS. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 2, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Lenexa, KS (United States)

Facility

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  • 1097599 (VAI Fri Jul 26 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1067224 (NAI Wed Sep 19 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 875737 (NAI Thu Apr 24 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources