FDA Inspection
Western Kentucky Regional Blood CtrWestern Kentucky Regional Blood Ctr – FDA Inspection, Jul 22, 2010
Record Details
This FDA Inspection record concerns Western Kentucky Regional Blood Ctr, with an inspection on July 22, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- July 22, 2010
- Product Type
- Biologics
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ID · 8dc8a0d8-f90a-49f1-94ef-afc42c44ba28
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 673323
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
1- 21 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs
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Other FDA inspections of Western Kentucky Regional Blood Ctr
6| Date | Classification | Office | Project area |
|---|---|---|---|
| March 24, 2026 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| August 30, 2021 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| June 6, 2018 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| March 9, 2016 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| January 14, 2014 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Western Kentucky Regional Blood Ctr
- FDA Inspection 1309978 - 2026-03-24
- FDA Inspection 1153258 - 2021-08-30
- FDA Inspection 1055333 - 2018-06-06
- FDA Inspection 962499 - 2016-03-09
- FDA Inspection 865140 - 2014-01-14
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