# Gyrus ACMI, Inc. – FDA Inspection, Sep 18, 2013

Source: https://www.keypedia.com/records/fda_inspections/gyrus-acmi-inc/c3e19e26-8fbd-4c81-94e1-d4e867e40ca0
Source feed: FDA_Inspections

> FDA inspection 848969 of Gyrus ACMI, Inc., September 18, 2013. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 848969
- Company Name: Gyrus ACMI, Inc.
- Inspection Date: 2013-09-18
- 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: 4

## Related Documents

- FDA Inspection 1170310 - 2022-05-02
- FDA Inspection 977394 - 2016-07-01
- FDA Inspection 683599 - 2010-09-15

Company: https://www.keypedia.com/companies/gyrus-acmi-inc/1135a75b-f1b4-41d1-8fdd-44a5b2891a6f

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