# FDA Inspection 675706 - Aesculap Inc - July 13, 2010

Source: https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/06c4f09e-61df-483d-8fae-a1eff3f3f6cc
Source feed: FDA_Inspections

> FDA Inspection 675706 for Aesculap Inc on July 13, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 675706
- Company Name: Aesculap Inc
- Inspection Date: 2010-07-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/aesculap-inc/40479973-1b19-440a-8e8c-5aeec6c45a29

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