# FDA Inspection 994818 - Maquet Medical Systems USA - September 29, 2016

Source: https://www.keypedia.com/records/fda_inspections/maquet-medical-systems-usa/d0531410-9f89-44ff-8450-ae5a56a0daaf
Source feed: FDA_Inspections

> FDA Inspection 994818 for Maquet Medical Systems USA on September 29, 2016. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 994818
- Company Name: Maquet Medical Systems USA
- Inspection Date: 2016-09-29
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 851698 - 2013-10-15](https://www.keypedia.com/records/fda_inspections/maquet-medical-systems-usa/41ef97fe-3077-4010-a6de-01da93885a68)
- [FDA Inspection 851698 - 2013-10-15](https://www.keypedia.com/records/fda_inspections/maquet-medical-systems-usa/4a30055e-d63b-496e-9254-cf556ff34c07)

Company: https://www.keypedia.com/companies/maquet-medical-systems-usa/05a2f1eb-196f-497e-bab0-83f1d16b0cf7

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