# FDA Inspection 678385 - Quest Medical, Inc. - August 27, 2010

Source: https://www.keypedia.com/records/fda_inspections/quest-medical-inc/26ed7d6b-9ac2-4e43-a7c7-63e63bbde659
Source feed: FDA_Inspections

> FDA Inspection 678385 for Quest Medical, Inc. on August 27, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 678385
- Company Name: Quest Medical, Inc.
- Inspection Date: 2010-08-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 892147 - 2014-08-22](https://www.keypedia.com/records/fda_inspections/quest-medical-inc/c6912436-69c0-4b4b-83ad-db57ecc5512e)
- [FDA Inspection 892147 - 2014-08-22](https://www.keypedia.com/records/fda_inspections/quest-medical-inc/3e836595-287a-481f-8f5e-b62cb0dc170a)
- [FDA Inspection 678385 - 2010-08-27](https://www.keypedia.com/records/fda_inspections/quest-medical-inc/9d280cb6-64d9-49e7-8865-c26c4cb9a939)

Company: https://www.keypedia.com/companies/quest-medical-inc/e6a0ecac-fe93-4b36-92d2-c19663a030d3

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