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FDA Inspection
•Biomat USA Inc•May 17, 2012

Biomat USA Inc – FDA Inspection, May 17, 2012

Record Details

This FDA Inspection record concerns Biomat USA Inc, with an inspection on May 17, 2012, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Biomat USA Inc
Inspection Date
May 17, 2012
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 4bd6cd19-b3ff-4a40-9402-d226dbd4d6f9

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
784315
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

1
  1. 21 CFR 606.170(a)Adverse Reaction- Reports of Investigations

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Biomat USA Inc

2
DateClassificationOfficeProject area
November 20, 2017VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 15, 2016VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for Biomat USA Inc
  • FDA Inspection 1031702 - 2017-11-20
  • FDA Inspection 983677 - 2016-08-15

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