# Alltech Medical Systems America Inc – FDA Inspection, Jun 17, 2009

Source: https://www.keypedia.com/records/fda_inspections/alltech-medical-systems-america-inc/a21d11a8-2f16-4e58-9d24-130db235e2e6
Source feed: FDA_Inspections

> FDA inspection 589973 of Alltech Medical Systems America Inc, June 17, 2009. Classification: Voluntary Action Indicated (VAI). 3 citations 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: 589973
- Company Name: Alltech Medical Systems America Inc
- Inspection Date: 2009-06-17
- 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: 3

## Related Documents

- [FDA Inspection 1097831 - 2019-07-29](https://www.keypedia.com/records/fda_inspections/alltech-medical-systems-america-inc/fb8f768c-8952-4941-a9bb-d188ba4eb700)
- FDA Inspection 827215 - 2013-03-21

Company: https://www.keypedia.com/companies/alltech-medical-systems-america-inc/239def2e-4814-4f48-91a6-c5498cc93e40

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