FDA Inspection
HRF, IncHRF, Inc – FDA Inspection, Nov 20, 2009
Record Details
This FDA Inspection record concerns HRF, Inc, with an inspection on November 20, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- HRF, Inc
- Inspection Date
- November 20, 2009
- Product Type
- Biologics
View Company Profile
ID · c4a6754d-2a71-49ad-9890-b787ef01429a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 630078
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
3- 21 CFR 606.65(e)Following manufacturer"s instructions
- 21 CFR 606.20(b)Qualifications of responsible personnel
- 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 HRF, Inc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| September 17, 2025 | Not classified | Atlanta District Office | |
| July 27, 2021 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| March 20, 2019 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| March 18, 2016 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| March 1, 2013 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for HRF, Inc
- FDA Inspection 1283202 - 2025-09-17
- FDA Inspection 1147778 - 2021-07-27
- FDA Inspection 1083359 - 2019-03-20
- FDA Inspection 963380 - 2016-03-18
- FDA Inspection 821175 - 2013-03-01
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