# CosmoFrance, Inc. – FDA Inspection, Oct 30, 2014

Source: https://www.keypedia.com/records/fda_inspections/cosmofrance-inc/dd8d0f5b-8c3a-4245-b784-0a61f358d1c0
Source feed: FDA_Inspections

> FDA inspection 910062 of CosmoFrance, Inc., October 30, 2014. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 910062
- Company Name: CosmoFrance, Inc.
- Inspection Date: 2014-10-30
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1151857 - 2021-09-16](https://www.keypedia.com/records/fda_inspections/cosmofrance-inc/555a4f68-3d46-4ea8-abdd-6dbd3e5955c0)
- [FDA Inspection 1084958 - 2019-04-02](https://www.keypedia.com/records/fda_inspections/cosmofrance-inc/f48ecfc0-14f4-40f5-9bc8-c3b2fff5a70f)

Company: https://www.keypedia.com/companies/cosmofrance-inc/7d90be73-0aee-4bbc-b296-8d1ba63e8ba2

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