# FDA Inspection 796781 - Aesculap Inc - August 30, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/fda53588-dd8f-4730-b112-4a3ea4d5503a/
Source feed: FDA_Inspections

> FDA Inspection 796781 for Aesculap Inc on August 30, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 796781
- Company Name: Aesculap Inc
- Inspection Date: 2012-08-30
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/aesculap-inc/d29d14e6-1cfa-415e-8172-44ad4aa1b329

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