FDA Inspection 1045305 — Distron Corporation
The FDA completed an inspection of Distron Corporation on Mar 15, 2018 in Attleboro Falls, MA. 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
- Mar 15, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Attleboro Falls, MA (United States)