# FDA Inspection 1055539 - Aesculap Inc - June 13, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/03807ef0-64bd-4fa8-817c-d642773f53f7
Source feed: FDA_Inspections

> FDA Inspection 1055539 for Aesculap Inc on June 13, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1055539
- Company Name: Aesculap Inc
- Inspection Date: 2018-06-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1055539 - 2018-06-13](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/678212a6-15b3-4fc5-9b1f-1ddf4d575cc9)
- [FDA Inspection 1055539 - 2018-06-13](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/c9f80ead-069e-45e5-89ad-16f17bab6bf2)
- [FDA Inspection 986649 - 2016-09-14](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/4b635ce7-8c7f-4165-98bd-53399fc1b387)
- [FDA Inspection 986649 - 2016-09-14](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/064ee17c-a107-4f3d-bedc-e6cedf2b65e7)
- [FDA Inspection 901818 - 2014-10-23](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/fd8cbe0e-eb20-4e24-a89a-fada494c5c18)

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