# Teledyne Flir Commercial Systems, Inc. – FDA Inspection, Jul 29, 2015

Source: https://www.keypedia.com/records/fda_inspections/teledyne-flir-commercial-systems-inc/cbe9e307-f976-427b-bcbc-ed8bf9772331
Source feed: FDA_Inspections

> FDA inspection 939046 of Teledyne Flir Commercial Systems, Inc., July 29, 2015. Classification: Voluntary Action Indicated (VAI). 2 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: 939046
- Company Name: Teledyne Flir Commercial Systems, Inc.
- Inspection Date: 2015-07-29
- 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: 2

## Related Documents

- [FDA Inspection 1181787 - 2022-10-04](https://www.keypedia.com/records/fda_inspections/teledyne-flir-commercial-systems-inc/2fe35be0-de19-4df6-a051-f5726f00f116)
- FDA Inspection 1058506 - 2018-06-27

Company: https://www.keypedia.com/companies/teledyne-flir-commercial-systems-inc/1f84d8af-18df-472d-914c-89b4c17ad269

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