# FDA Inspection 598265 - Ned Michael Foght - July 15, 2009

Source: https://www.keypedia.com/records/fda_inspections/ned-michael-foght/82740edb-babc-4cf1-a1f5-879a5c95de69
Source feed: FDA_Inspections

> FDA Inspection 598265 for Ned Michael Foght on July 15, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 598265
- Company Name: Ned Michael Foght
- Inspection Date: 2009-07-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 598265 - 2009-07-15](https://www.keypedia.com/records/fda_inspections/ned-michael-foght/43af972f-54a7-466c-b79a-d59b584387d4)

Company: https://www.keypedia.com/companies/ned-michael-foght/f3230f76-b347-4fa8-952c-6c6b897eeb6e

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