FDA Inspection 679601 — The Foredom Electric Co.
The FDA completed an inspection of The Foredom Electric Co. on Sep 1, 2010 in Bethel, CT. 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
- Sep 1, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Bethel, CT (United States)