# Gyrus Acmi, In. – FDA Inspection, Jun 11, 2013

Source: https://www.keypedia.com/records/fda_inspections/gyrus-acmi-in/bf2344e6-6053-4ea2-b131-848d165429a9
Source feed: FDA_Inspections

> FDA inspection 837099 of Gyrus Acmi, In., June 11, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 803. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 837099
- Company Name: Gyrus Acmi, In.
- Inspection Date: 2013-06-11
- 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: 2

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- FDA Inspection 668592 - 2010-06-24

Company: https://www.keypedia.com/companies/gyrus-acmi-in/8b143956-34ad-4a45-8d6c-4e93b2479e31

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