# FDA Inspection 1110285 - Tecomet, Inc. - November 15, 2019

Source: https://www.keypedia.com/records/fda_inspections/tecomet-inc/e4c313e0-375f-4a7f-945f-08077ad34477
Source feed: FDA_Inspections

> FDA Inspection 1110285 for Tecomet, Inc. on November 15, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1110285
- Company Name: Tecomet, Inc.
- Inspection Date: 2019-11-15
- 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/tecomet-inc/3edd907b-3baf-4433-bdbe-af417a02a831

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