# Alltech Medical Systems America Inc – FDA Inspection, Jul 29, 2019

Source: https://www.keypedia.com/records/fda_inspections/alltech-medical-systems-america-inc/fb8f768c-8952-4941-a9bb-d188ba4eb700
Source feed: FDA_Inspections

> FDA inspection 1097831 of Alltech Medical Systems America Inc, July 29, 2019. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1097831
- Company Name: Alltech Medical Systems America Inc
- Inspection Date: 2019-07-29
- 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: 8

## Related Documents

- FDA Inspection 827215 - 2013-03-21
- [FDA Inspection 589973 - 2009-06-17](https://www.keypedia.com/records/fda_inspections/alltech-medical-systems-america-inc/a21d11a8-2f16-4e58-9d24-130db235e2e6)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/laureen-m-geniusz/759a858e-e3f3-4c48-8194-9804c7ab2a7b)

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