FDA Inspection 1103492 — Dynamo
The FDA completed an inspection of Dynamo on Jul 23, 2019 in Lithia, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Jul 23, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Lithia, FL (United States)