# FDA Inspection 852042 - CFL Industries, Inc. - September 30, 2013

Source: https://www.keypedia.com/records/fda_inspections/cfl-industries-inc/12f9c115-db7e-4d8f-a48a-e58baed4474f
Source feed: FDA_Inspections

> FDA Inspection 852042 for CFL Industries, Inc. on September 30, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 852042
- Company Name: CFL Industries, Inc.
- Inspection Date: 2013-09-30
- 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 852042 - 2013-09-30](https://www.keypedia.com/records/fda_inspections/cfl-industries-inc/66238113-3493-45f6-8967-78288cbeea0d)

Company: https://www.keypedia.com/companies/cfl-industries-inc/f2648e75-9e35-4309-b055-9e52d0f1e421

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