# FDA Inspection 1115307 - Tecomet Inc. - January 09, 2020

Source: https://www.globalkeysolutions.net/records/fda_inspections/tecomet-inc/bc3f8adb-52e6-43ae-9f76-ebf8a4b4c290
Source feed: FDA_Inspections

> FDA Inspection 1115307 for Tecomet Inc. on January 09, 2020. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1115307
- Company Name: Tecomet Inc.
- Inspection Date: 2020-01-09
- 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 1115307 - 2020-01-09](https://www.globalkeysolutions.net/records/fda_inspections/tecomet-inc/83e133a1-6b97-4e74-84a7-c3da4f306433)
- [FDA Inspection 945863 - 2015-09-23](https://www.globalkeysolutions.net/records/fda_inspections/tecomet-inc/57f84152-8617-407d-a2e9-5c3ef6b2638b)
- [FDA Inspection 661409 - 2010-05-13](https://www.globalkeysolutions.net/records/fda_inspections/tecomet-inc/9529fe9d-ecf3-429e-a044-f503cd09db02)

Company: https://www.globalkeysolutions.net/companies/tecomet-inc/1135970d-7a63-4e05-9b75-157100285ac4

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