# Gyrus ACMI, Inc. – FDA Inspection, Jun 14, 2012

Source: https://www.keypedia.com/records/fda_inspections/gyrus-acmi-inc/1f770ace-4963-43eb-90dc-ff61e9676223
Source feed: FDA_Inspections

> FDA inspection 789809 of Gyrus ACMI, Inc., June 14, 2012. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 789809
- Company Name: Gyrus ACMI, Inc.
- Inspection Date: 2012-06-14
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1055329 - 2018-05-23
- [FDA Inspection 1048537 - 2018-04-17](https://www.keypedia.com/records/fda_inspections/gyrus-acmi-inc/30c7858f-52e3-435b-a5ed-183917e0df20)
- FDA Inspection 920803 - 2015-04-03
- FDA Inspection 840684 - 2013-06-21
- FDA Inspection 731008 - 2011-06-13

Company: https://www.keypedia.com/companies/gyrus-acmi-inc/bf4bfaf5-665f-4f80-a65e-733a5eb56fa4

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