FDA Inspection 1270003 — Bio-Rad
The FDA completed an inspection of Bio-Rad on May 16, 2025 in Steenvoorde. 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
- May 16, 2025
- Fiscal Year
- 2025
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Steenvoorde (France)
Citations
| ID | CFR | Description |
|---|---|---|
| 3434 | 21 CFR 820.75(c) | Documentation - review in response to changes or deviations |