# FDA Inspection 679601 - The Foredom Electric Co. - September 01, 2010

Source: https://www.keypedia.com/records/fda_inspections/the-foredom-electric-co/4c00d208-a107-45cf-9933-2f4716870f00
Source feed: FDA_Inspections

> FDA Inspection 679601 for The Foredom Electric Co. on September 01, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 679601
- Company Name: The Foredom Electric Co.
- Inspection Date: 2010-09-01
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 818245 - 2013-02-07](https://www.keypedia.com/records/fda_inspections/the-foredom-electric-co/b7f0eae9-20ac-415c-b271-a8a63036ac39)

Company: https://www.keypedia.com/companies/the-foredom-electric-co/ae55c061-06ab-4744-b04a-5d56c92ba699

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7