# Gyrus ACMI, Inc. – FDA Inspection, Apr 17, 2018

Source: https://www.keypedia.com/records/fda_inspections/gyrus-acmi-inc/30c7858f-52e3-435b-a5ed-183917e0df20
Source feed: FDA_Inspections

> FDA inspection 1048537 of Gyrus ACMI, Inc., April 17, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1048537
- Company Name: Gyrus ACMI, Inc.
- Inspection Date: 2018-04-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- 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
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- FDA Inspection 840684 - 2013-06-21
- [FDA Inspection 789809 - 2012-06-14](https://www.keypedia.com/records/fda_inspections/gyrus-acmi-inc/1f770ace-4963-43eb-90dc-ff61e9676223)
- FDA Inspection 731008 - 2011-06-13

## Related Officers

- [Company Rep](https://www.keypedia.com/people/sunitha-k-rajaram/1a0872d4-5e7b-4690-a2be-3877aec25053)

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