# Gyrus ACMI, Inc. – FDA Inspection, Dec 11, 2015

Source: https://www.keypedia.com/records/fda_inspections/gyrus-acmi-inc/f14d513c-5b14-43a3-91b7-d728755f766b
Source feed: FDA_Inspections

> FDA inspection 952450 of Gyrus ACMI, Inc., December 11, 2015. Classification: No Action Indicated (NAI). 6 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 952450
- Company Name: Gyrus ACMI, Inc.
- Inspection Date: 2015-12-11
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1295532 - 2025-11-12](https://www.keypedia.com/records/fda_inspections/gyrus-acmi-inc/ff3b286d-2be9-4dc9-a51c-c94a80f08fab)
- FDA Inspection 1116173 - 2020-01-14
- FDA Inspection 1020250 - 2017-07-27
- FDA Inspection 920049 - 2015-03-20
- FDA Inspection 798492 - 2012-08-31

Company: https://www.keypedia.com/companies/gyrus-acmi-inc/cc021f12-0ca9-4ff6-b22a-d5cdd858904d

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