# Avotec, Inc. – FDA Inspection, Jan 12, 2018

Source: https://www.keypedia.com/records/fda_inspections/avotec-inc/4270046d-ec62-465f-a72f-e6a9624cd704
Source feed: FDA_Inspections

> FDA inspection 1037667 of Avotec, Inc., January 12, 2018. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR parts 803 and 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1037667
- Company Name: Avotec, Inc.
- Inspection Date: 2018-01-12
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

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- [FDA Inspection 1196089 - 2023-01-27](https://www.keypedia.com/records/fda_inspections/avotec-inc/ec04ea29-2add-4604-bf34-889333666f71)
- FDA Inspection 935262 - 2015-07-21
- FDA Inspection 754052 - 2011-11-15

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/karen-m-cruz-arenas/6c698301-84ca-4ba7-a79c-309721db2f1b)

Company: https://www.keypedia.com/companies/avotec-inc/c9e64cf4-dc73-4c66-b692-3ef7516ed465

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