# FDA Inspection 939850 - Aesculap AG - July 16, 2015

Source: https://www.keypedia.com/records/fda_inspections/aesculap-ag/03e92ed6-9fa2-4e98-b2a1-97bf03b965cf
Source feed: FDA_Inspections

> FDA Inspection 939850 for Aesculap AG on July 16, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 939850
- Company Name: Aesculap AG
- Inspection Date: 2015-07-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/aesculap-ag/7bf23acc-23fe-4733-bd67-2e0736286f2f

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