FDA Inspection
KEDPLASMA LLCKEDPLASMA LLC – FDA Inspection, Aug 30, 2018
Record Details
This FDA Inspection record concerns KEDPLASMA LLC, with an inspection on August 30, 2018, issued by the Center for Biologics Evaluation and Research, covering biologics.
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ID · bc508a66-a380-4abf-994d-94db67367253
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1063846
- FDA center
- Biologics
- Project area
- Blood and Blood Products
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 606.40(a)(3)Provide space for storage of blood & blood products
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Other FDA inspections of KEDPLASMA LLC
1| Date | Classification | Office | Project area |
|---|---|---|---|
| May 17, 2012 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
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