# Aesculap AG – FDA Inspection, Jun 7, 2018

Source: https://www.keypedia.com/records/fda_inspections/aesculap-ag/9df33de5-3680-487a-ac21-a07699d6e643
Source feed: FDA_Inspections

> FDA inspection 1078171 of Aesculap AG, June 07, 2018. Form 483 issued. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1078171
- Company Name: Aesculap AG
- Inspection Date: 2018-06-07
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- 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 987720 - 2016-09-22
- FDA Inspection 939850 - 2015-07-16
- FDA Inspection 841575 - 2013-07-04
- FDA Inspection 809376 - 2012-12-04

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

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8