# Aesculap Inc - Inspection Records

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

> Inspection records and compliance data for Aesculap Inc in Hazelwood, Missouri. Access full analysis and detailed observations.

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## Details

- Name: Aesculap Inc
- FEI Number: 3003587896
- City: Hazelwood
- State: Missouri
- Country Name: United States
- Address Line 1: 615 Lambert Pointe Dr
- Zip Code: 63042

## Related Documents

- [483 - Aesculap Inc - 2019-10-30](https://www.globalkeysolutions.net/records/483/aesculap-inc/ce23b678-4e21-4660-9a07-aeb4b4cd0ec2) — source: FDA, date: October 30, 2019
- [483 - Aesculap Inc - 2018-06-13](https://www.globalkeysolutions.net/records/483/aesculap-inc/84d3fe67-45a3-4d41-95c4-3f0f3841c6c0) — source: FDA, date: June 13, 2018
- [FDA Inspection 1055539 - Aesculap Inc - 2018-06-13](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/678212a6-15b3-4fc5-9b1f-1ddf4d575cc9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 13, 2018
- [FDA Inspection 1055539 - Aesculap Inc - 2018-06-13](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/03807ef0-64bd-4fa8-817c-d642773f53f7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 13, 2018
- [FDA Inspection 1055539 - Aesculap Inc - 2018-06-13](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/c9f80ead-069e-45e5-89ad-16f17bab6bf2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 13, 2018
- [FDA Inspection 986649 - Aesculap Inc - 2016-09-14](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/064ee17c-a107-4f3d-bedc-e6cedf2b65e7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 14, 2016
- [FDA Inspection 986649 - Aesculap Inc - 2016-09-14](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/4b635ce7-8c7f-4165-98bd-53399fc1b387) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 14, 2016
- [FDA Inspection 901818 - Aesculap Inc - 2014-10-23](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/38b81622-d174-4c8a-9f2f-c60d44aa365f) — classification: No Action Indicated (NAI), source: FDA, date: October 23, 2014
- [FDA Inspection 901818 - Aesculap Inc - 2014-10-23](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/fd8cbe0e-eb20-4e24-a89a-fada494c5c18) — classification: No Action Indicated (NAI), source: FDA, date: October 23, 2014
- [FDA Inspection 843597 - Aesculap Inc - 2013-08-09](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/9a5e1f4b-579d-4b75-af71-b1c6c99e8253) — classification: No Action Indicated (NAI), source: FDA, date: August 9, 2013
- [FDA Inspection 675706 - Aesculap Inc - 2010-07-13](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/06c4f09e-61df-483d-8fae-a1eff3f3f6cc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 13, 2010

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