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FDA Inspection
•Biomat USA Inc•May 6, 2010

Biomat USA Inc – FDA Inspection, May 6, 2010

Record Details

This FDA Inspection record concerns Biomat USA Inc, with an inspection on May 6, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Biomat USA Inc
Inspection Date
May 6, 2010
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 1d5c08b1-1168-44b6-8abe-76086c166918

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
661175
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

1
  1. 21 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Biomat USA Inc

5
DateClassificationOfficeProject area
July 27, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
November 25, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 17, 2014NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
November 15, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 17, 2012NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for Biomat USA Inc
  • FDA Inspection 1062339 - 2018-07-27
  • FDA Inspection 950741 - 2015-11-25
  • FDA Inspection 887239 - 2014-07-17
  • FDA Inspection 855254 - 2013-11-15
  • FDA Inspection 794963 - 2012-08-17

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