# FDA Inspection 1013359 - Infraredx, Inc. - June 02, 2017

Source: https://www.keypedia.com/records/fda_inspections/infraredx-inc/cadd3583-dd2e-4c87-bc9e-2fdea4c48fcd
Source feed: FDA_Inspections

> FDA Inspection 1013359 for Infraredx, Inc. on June 02, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1013359
- Company Name: Infraredx, Inc.
- Inspection Date: 2017-06-02
- 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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Company: https://www.keypedia.com/companies/infraredx-inc/5f598ed1-9b87-414f-89b6-347cb8ce82c9

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