# FDA Inspection 1032209 - Temrex  Corporation - November 21, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/temrex-corporation/b69b70e3-c933-4435-bd2b-1bf53719ed37
Source feed: FDA_Inspections

> FDA Inspection 1032209 for Temrex  Corporation on November 21, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1032209
- Company Name: Temrex  Corporation
- Inspection Date: 2017-11-21
- 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.globalkeysolutions.net/companies/temrex-corporation/7cbfbd89-c98d-47c9-a62b-685dd0bb98cc

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