# FDA Inspection 1058506 - Teledyne Flir Commercial Systems, Inc. - June 27, 2018

Source: https://www.keypedia.com/records/fda_inspections/teledyne-flir-commercial-systems-inc/129e4b7e-55f8-49fc-8a1d-cb5991f0c0eb
Source feed: FDA_Inspections

> FDA Inspection 1058506 for Teledyne Flir Commercial Systems, Inc. on June 27, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1058506
- Company Name: Teledyne Flir Commercial Systems, Inc.
- Inspection Date: 2018-06-27
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [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](https://www.keypedia.com/records/fda_inspections/teledyne-flir-commercial-systems-inc/e4387b3c-588b-48c8-b898-90c23e06d98a)
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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
