# FDA Inspection 1088788 - Tecomet, Inc. - May 07, 2019

Source: https://www.keypedia.com/records/fda_inspections/tecomet-inc/49127b36-14de-483d-a644-c5af551232a2
Source feed: FDA_Inspections

> FDA Inspection 1088788 for Tecomet, Inc. on May 07, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1088788
- Company Name: Tecomet, Inc.
- Inspection Date: 2019-05-07
- 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 1088788 - 2019-05-07](https://www.keypedia.com/records/fda_inspections/tecomet-inc/63c5cb09-fdc6-4846-990f-756e2f5e15e7)

Company: https://www.keypedia.com/companies/tecomet-inc/c00229cb-b05f-414b-bd9b-93bc169dc8d2

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