FDA Inspection 1063846 — KEDPLASMA LLC
The FDA completed an inspection of KEDPLASMA LLC on Aug 30, 2018 in Flagstaff, AZ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Biologics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Aug 30, 2018
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Flagstaff, AZ (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 43 | 21 CFR 606.40(a)(3) | Provide space for storage of blood & blood products |