# FDA Inspection 1115308 - Tecomet Inc. - January 13, 2020

Source: https://www.keypedia.com/records/fda_inspections/tecomet-inc/c66597d4-a6f0-4b95-88da-4ed07aa352fa
Source feed: FDA_Inspections

> FDA Inspection 1115308 for Tecomet Inc. on January 13, 2020. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1115308
- Company Name: Tecomet Inc.
- Inspection Date: 2020-01-13
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1115308 - 2020-01-13](https://www.keypedia.com/records/fda_inspections/tecomet-inc/562a250c-ec89-4764-b61e-211ab14a36ff)

Company: https://www.keypedia.com/companies/tecomet-inc/d60e39bd-5b24-4443-ac72-ae149eee3c5b

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