FDA Inspection 1089214 — VentureMed Group, Inc.
The FDA completed an inspection of VentureMed Group, Inc. on April 18, 2019 in Plymouth, 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
- April 18, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Plymouth, MN (United States)