FDA Inspection 603357 — Kedplasma LLC
The FDA completed an inspection of Kedplasma LLC on July 21, 2009 in Houston, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Biologics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- July 21, 2009
- Fiscal Year
- 2009
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Houston, TX (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 144 | 21 CFR 606.140(c) | Adequate identification and handling of test samples |
| 353 | 21 CFR 640.68(b) | Final container |