# Maquet Cardiopulmonary GmbH – FDA Inspection, Aug 15, 2013

Source: https://www.keypedia.com/records/fda_inspections/maquet-cardiopulmonary-gmbh/9a7af37a-325b-42a0-bedf-e0b004f8490e
Source feed: FDA_Inspections

> FDA inspection 857072 of Maquet Cardiopulmonary GmbH, August 15, 2013. Classification: Official Action Indicated (OAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 857072
- Company Name: Maquet Cardiopulmonary GmbH
- Inspection Date: 2013-08-15
- 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: 0

## Related Documents

- [FDA Inspection 1174429 - 2022-06-24](https://www.keypedia.com/records/fda_inspections/maquet-cardiopulmonary-gmbh/c98459a5-2c03-48f3-9592-f6a07bc488ce)
- [FDA Inspection 857077 - 2013-09-23](https://www.keypedia.com/records/fda_inspections/maquet-cardiopulmonary-gmbh/527071ae-001a-4a20-b912-31733c2b7ff3)

Company: https://www.keypedia.com/companies/maquet-cardiopulmonary-gmbh/21b3de69-3682-4f19-8aec-1cfee4b55c0a

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