# FDA Inspection 673630 - Quick Point Inc - July 23, 2010

Source: https://www.keypedia.com/records/fda_inspections/quick-point-inc/3d094b2e-5b9c-4413-8c66-285fcb5501b3
Source feed: FDA_Inspections

> FDA Inspection 673630 for Quick Point Inc on July 23, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 673630
- Company Name: Quick Point Inc
- Inspection Date: 2010-07-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 673630 - 2010-07-23](https://www.keypedia.com/records/fda_inspections/quick-point-inc/207913c0-c37f-42cb-8f45-654d1d5742f9)

Company: https://www.keypedia.com/companies/quick-point-inc/d5e37580-6be1-46e4-84ed-d44db90683ec

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