# Tecomet, Inc. – FDA Inspection, Apr 18, 2024

Source: https://www.keypedia.com/records/fda_inspections/tecomet-inc/200d99c8-4084-4c61-a683-beb40a0843ff
Source feed: FDA_Inspections

> FDA inspection 1236273 of Tecomet, Inc., April 18, 2024. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1236273
- Company Name: Tecomet, Inc.
- Inspection Date: 2024-04-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1110285 - 2019-11-15
- FDA Inspection 948437 - 2015-10-09

## Related Officers

- [Company Rep](https://www.keypedia.com/people/matthew-m-vernon/f77e8c18-8614-49e3-9b19-3327b7fe7648)

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