# 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 of Maquet Medical Systems USA, September 29, 2016. Classification: Official Action Indicated (OAI). 5 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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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)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- [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