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FDA Inspection 669134 — Biomat USA, Inc

Biomat USA, Inc — FEI 3003826898

The FDA completed an inspection of Biomat USA, Inc on June 25, 2010 in Fort Worth, TX. 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
June 25, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fort Worth, TX (United States)

Facility

Other inspections at this facility

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  • 1026015 (NAI Wed Jun 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 922269 (NAI Wed Apr 15 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 852553 (NAI Thu Oct 24 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 737675 (NAI Wed Jul 27 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources