# FDA Inspection 795673 - Creative Response Inc. - July 27, 2012

Source: https://www.keypedia.com/records/fda_inspections/creative-response-inc/4065260d-6be6-41ba-a0c3-5e1946ee5099
Source feed: FDA_Inspections

> FDA Inspection 795673 for Creative Response Inc. on July 27, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 795673
- Company Name: Creative Response Inc.
- Inspection Date: 2012-07-27
- 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 795673 - 2012-07-27](https://www.keypedia.com/records/fda_inspections/creative-response-inc/b8175796-72fa-4e66-9a40-de5ff43bc2c5)

Company: https://www.keypedia.com/companies/creative-response-inc/28d7e945-bd26-472a-9a0c-405825bb7d4e

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