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FDA Inspection
•Biomat USA, Inc.•October 18, 2018

Biomat USA, Inc. – FDA Inspection, Oct 18, 2018

Record Details

This FDA Inspection record concerns Biomat USA, Inc., with an inspection on October 18, 2018, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Biomat USA, Inc.
Inspection Date
October 18, 2018
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
People
  • Kathryn A. Krentz (Company Rep)
  • Leeterry Moore (Issuing Officer)
View Company Profile

ID · 50f2f7ed-a3fb-498e-a0af-1f0360d52951

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1071044
FDA center
Biologics
Project area
Blood and Blood Products

Other FDA inspections of Biomat USA, Inc.

4
DateClassificationOfficeProject area
October 6, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 5, 2014NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 24, 2012VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 23, 2010VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for Biomat USA, Inc.
  • FDA Inspection 988681 - 2016-10-06
  • FDA Inspection 865425 - 2014-02-05
  • FDA Inspection 785185 - 2012-04-24
  • FDA Inspection 669894 - 2010-06-23

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