# FDA Inspection 909310 - C&E GP Specialists Inc. - August 06, 2014

Source: https://www.keypedia.com/records/fda_inspections/ce-gp-specialists-inc/f5d4f4f9-ad65-47b0-9db4-514d474505f8
Source feed: FDA_Inspections

> FDA Inspection 909310 for C&E GP Specialists Inc. on August 06, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 909310
- Company Name: C&E GP Specialists Inc.
- Inspection Date: 2014-08-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1181831 - 2022-09-19](https://www.keypedia.com/records/fda_inspections/ce-gp-specialists-inc/37d5aa77-65ca-41ea-86ad-011269b22627)

Company: https://www.keypedia.com/companies/ce-gp-specialists-inc/af1c9156-0ad1-44f0-914f-595d6f5ca8ae

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