FDA Inspection 680056 — Diasorin Inc.
The FDA completed an inspection of Diasorin Inc. on September 27, 2010 in Stillwater, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- September 27, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Stillwater, MN (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 4208 | 21 CFR 806.20(a) | Records not kept |