# Teco Diagnostics, Inc. – FDA Inspection, May 9, 2018

Source: https://www.keypedia.com/records/fda_inspections/teco-diagnostics-inc/7d647221-f055-4a90-9d3a-e86390c0c583
Source feed: FDA_Inspections

> FDA inspection 1052273 of Teco Diagnostics, Inc., May 09, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1052273
- Company Name: Teco Diagnostics, Inc.
- Inspection Date: 2018-05-09
- 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: 3

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- [FDA Inspection 753658 - 2011-10-14](https://www.keypedia.com/records/fda_inspections/teco-diagnostics-inc/8cc7bffd-30cd-4236-9df9-2a7ddde902f0)
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## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/sonya-l-karsik/c24603b9-5ca0-46f5-861a-b367155b0def)

Company: https://www.keypedia.com/companies/teco-diagnostics-inc/af419fbf-c322-4adf-aecc-a990816d70bb

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