FDA Inspection 980290 — Dymedix Diagnostics, Inc.
The FDA completed an inspection of Dymedix Diagnostics, Inc. on July 7, 2016 in Shoreview, 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
- July 7, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Shoreview, MN (United States)