FDA Inspection
Kedplasma LLCKedplasma LLC – FDA Inspection, Jul 21, 2009
Record Details
This FDA Inspection record concerns Kedplasma LLC, with an inspection on July 21, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Kedplasma LLC
- Inspection Date
- July 21, 2009
- Product Type
- Biologics
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ID · 74c3c6ac-45e8-47a6-bbb2-9151408f7570
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 603357
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
2- 21 CFR 606.140(c)Adequate identification and handling of test samples
- 21 CFR 640.68(b)Final container
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Other FDA inspections of Kedplasma LLC
5| Date | Classification | Office | Project area |
|---|---|---|---|
| December 6, 2022 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| April 18, 2017 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| March 11, 2015 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| April 25, 2013 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| August 3, 2011 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Kedplasma LLC
- FDA Inspection 1195344 - 2022-12-06
- FDA Inspection 1010200 - 2017-04-18
- FDA Inspection 919561 - 2015-03-11
- FDA Inspection 831133 - 2013-04-25
- FDA Inspection 742311 - 2011-08-03
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