# FDA Inspection 672612 - Refractec LLC - June 17, 2010

Source: https://www.keypedia.com/records/fda_inspections/refractec-llc/0a478d8c-85a3-4c94-9954-bcff2739eeef
Source feed: FDA_Inspections

> FDA Inspection 672612 for Refractec LLC on June 17, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 672612
- Company Name: Refractec LLC
- Inspection Date: 2010-06-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 672612 - 2010-06-17](https://www.keypedia.com/records/fda_inspections/refractec-llc/79966c79-3e12-4cf0-a4cb-d2d786071534)

Company: https://www.keypedia.com/companies/refractec-llc/4a285181-cd7f-4908-9290-56bf74cca55b

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