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FDA Inspection 981293 — Biomat USA, Inc.

Biomat USA, Inc. — FEI 3006293236

The FDA completed an inspection of Biomat USA, Inc. on August 4, 2016 in Corpus Christi, 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
August 4, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Corpus Christi, TX (United States)

Facility

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  • 891827 (NAI Tue Aug 19 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 768776 (NAI Fri Feb 10 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
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FDA data resources