FDA Inspection 578579 — Sirtex Wilmington LLC
The FDA completed an inspection of Sirtex Wilmington LLC on Jan 30, 2009 in Wilmington, MA. 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: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jan 30, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Wilmington, MA (United States)
Additional Details
Postmarket Audit Inspections
Citations
| ID | CFR | Description |
|---|---|---|
| 731 | 21 CFR 803.50(a)(1) | Report of Death or Serious Injury |