FDA Inspection 1102921 — Virtex
The FDA completed an inspection of Virtex on September 12, 2019 in Anoka, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- September 12, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Anoka, MN (United States)