# FDA Inspection 670812 - Maquet Cardiovascular - June 28, 2010

Source: https://www.keypedia.com/records/fda_inspections/maquet-cardiovascular/7e598f11-3d41-4284-b2a8-ca15bd9981b1
Source feed: FDA_Inspections

> FDA Inspection 670812 for Maquet Cardiovascular on June 28, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 670812
- Company Name: Maquet Cardiovascular
- Inspection Date: 2010-06-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/maquet-cardiovascular/ac9dff1e-3528-415c-bbe8-b31ca18bf545

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