# FDA Inspection 980899 - Gyrus ACMI, Inc. - August 17, 2016

Source: https://www.keypedia.com/records/fda_inspections/gyrus-acmi-inc/5b352363-b915-43ee-b535-8faeaa3a0ab8
Source feed: FDA_Inspections

> FDA Inspection 980899 for Gyrus ACMI, Inc. on August 17, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 980899
- Company Name: Gyrus ACMI, Inc.
- Inspection Date: 2016-08-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/gyrus-acmi-inc/83de7ea8-de1b-4b07-805a-975da3d94ea6

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