FDA Inspection
Biomat USA IncBiomat USA Inc – FDA Inspection, Feb 1, 2010
Record Details
This FDA Inspection record concerns Biomat USA Inc, with an inspection on February 1, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Biomat USA Inc
- Inspection Date
- February 1, 2010
- Product Type
- Biologics
View Company Profile
ID · b747dcd8-092f-4382-b105-174465c7427f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 642601
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
3- 21 CFR 600.14(c)When to report
- 21 CFR 630.40(a)Notification
- 21 CFR 606.171Biological product deviation report
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Biomat USA Inc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| June 23, 2022 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| August 24, 2018 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| June 30, 2015 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| September 27, 2013 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| August 17, 2011 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Biomat USA Inc
- FDA Inspection 1173782 - 2022-06-23
- FDA Inspection 1063182 - 2018-08-24
- FDA Inspection 932372 - 2015-06-30
- FDA Inspection 850538 - 2013-09-27
- FDA Inspection 739997 - 2011-08-17
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