# FDA Inspection 1221779 - Gyrus ACMI, Inc. - November 02, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/gyrus-acmi-inc/fe9085a2-81a2-4d96-aca0-01d4a7337da9/
Source feed: FDA_Inspections

> FDA Inspection 1221779 for Gyrus ACMI, Inc. on November 02, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1221779
- Company Name: Gyrus ACMI, Inc.
- Inspection Date: 2023-11-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1221779 - 2023-11-02](https://www.globalkeysolutions.net/api/records/fda_inspections/gyrus-acmi-inc/0f105e4b-7602-422b-a265-dea37fd5e826/)
- [FDA Inspection 980899 - 2016-08-17](https://www.globalkeysolutions.net/api/records/fda_inspections/gyrus-acmi-inc/5b352363-b915-43ee-b535-8faeaa3a0ab8/)

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

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