# Corflex, Inc. – FDA Inspection, Jan 4, 2017

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

> FDA inspection 997339 of Corflex, Inc., January 04, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Officers

- Issuing Officer

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