# Aesculap AG – FDA Inspection, May 19, 2011

Source: https://www.keypedia.com/records/fda_inspections/aesculap-ag/82a8b036-6293-4bf3-8ef0-4d677828f993
Source feed: FDA_Inspections

> FDA inspection 729096 of Aesculap AG, May 19, 2011. Classification: Official Action Indicated (OAI). 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 729096
- Company Name: Aesculap AG
- Inspection Date: 2011-05-19
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1178394 - 2022-07-21](https://www.keypedia.com/records/fda_inspections/aesculap-ag/c301202a-fd12-4f51-912f-3075d36b9ada)
- [FDA Inspection 1078171 - 2018-06-07](https://www.keypedia.com/records/fda_inspections/aesculap-ag/9df33de5-3680-487a-ac21-a07699d6e643)
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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