# Aesculap Inc - Inspection Records

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

> Inspection records and compliance data for Aesculap Inc in Center Valley, Pennsylvania. Access full analysis and detailed observations.

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## Details

- Name: Aesculap Inc
- FEI Number: 2916714
- City: Center Valley
- State: Pennsylvania
- Country Name: United States
- Address Line 1: 3773 Corporate Pkwy
- Zip Code: 18034

## Related Documents

- [FDA Inspection 1277866 - Aesculap Inc - 2025-07-11](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/a5876d6b-becc-401b-a916-6f11e9141768) — source: FDA, date: July 11, 2025
- [FDA Inspection 1277866 - Aesculap Inc - 2025-07-11](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/d35e8401-e05b-484f-8018-2cf7133606fd) — classification: No Action Indicated (NAI), source: FDA, date: July 11, 2025
- [483 - Aesculap Inc - 2021-08-11](https://www.globalkeysolutions.net/records/483/aesculap-inc/46300e90-9d01-48f2-bcd0-2636d6a63be8) — source: FDA, date: August 11, 2021
- [FDA Inspection 1148504 - Aesculap Inc - 2021-08-11](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/4793f63a-ef2b-47b7-a8b3-4bb2f672e54f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 11, 2021
- [FDA Inspection 1148504 - Aesculap Inc - 2021-08-11](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/1cada70d-7b1b-4a4c-ab7f-825bce159a0b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 11, 2021
- [FDA Inspection 977569 - Aesculap Inc - 2016-07-13](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/5b284aa9-58bd-453d-8af4-1befe163dfbd) — classification: No Action Indicated (NAI), source: FDA, date: July 13, 2016
- [FDA Inspection 977569 - Aesculap Inc - 2016-07-13](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/b5de35be-5f1a-4130-98f7-b9d1eb1a17cf) — classification: No Action Indicated (NAI), source: FDA, date: July 13, 2016
- [FDA Inspection 924973 - Aesculap Inc - 2015-05-05](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/a0dac949-5175-4491-a828-dde9c946b887) — classification: No Action Indicated (NAI), source: FDA, date: May 5, 2015
- [FDA Inspection 924973 - Aesculap Inc - 2015-05-05](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/b31c7aea-4525-457e-9ce1-8cdd42eb8f9c) — classification: No Action Indicated (NAI), source: FDA, date: May 5, 2015
- [FDA Inspection 828602 - Aesculap Inc - 2013-04-24](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/2709437a-c7bf-4a97-a1b0-d7273810719c) — classification: No Action Indicated (NAI), source: FDA, date: April 24, 2013
- [FDA Inspection 822299 - Aesculap Inc - 2013-03-12](https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/b0482442-2513-47df-bfd8-9752c227312b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 12, 2013

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