FDA Inspection 675546 — Vitalant
The FDA completed an inspection of Vitalant on Jul 21, 2010 in Spokane, WA. 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). 3 citations were issued during this inspection. Product area: Biologics.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jul 21, 2010
- Fiscal Year
- 2010
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Spokane, WA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 212 | 21 CFR 640.3(b)(3) | Qualifications of donor - hemoglobin |
| 76 | 21 CFR 606.100(b) | Establish, maintain and follow manufacturing SOPs |
| 98 | 21 CFR 606.100(c) | Thorough investigations |