# FDA Inspection 997339 - Corflex, Inc. - January 04, 2017

Source: https://www.keypedia.com/records/fda_inspections/corflex-inc/740c9446-a019-4be3-acc1-754b81c2337a
Source feed: FDA_Inspections

> FDA Inspection 997339 for Corflex, Inc. on January 04, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 997339
- Company Name: Corflex, Inc.
- Inspection Date: 2017-01-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/corflex-inc/8666c05f-6c13-4eed-8d63-639e7385ef3e

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