FDA Inspection 808650 — Vitalant
The FDA completed an inspection of Vitalant on Nov 9, 2012 in Cheyenne, WY. 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
- Nov 9, 2012
- Fiscal Year
- 2013
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Cheyenne, WY (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 255 | 21 CFR 640.31 | Donor eligibility |