FDA Inspection 1029220 — Diatron US Inc.
The FDA completed an inspection of Diatron US Inc. on September 6, 2017 in Medley, FL. 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 6, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Medley, FL (United States)