# Aesculap Implant Systems LLC – FDA Inspection, Mar 4, 2015

Source: https://www.keypedia.com/records/fda_inspections/aesculap-implant-systems-llc/e1ae88cf-a5bd-49da-932e-9f54d5bac3dc
Source feed: FDA_Inspections

> FDA inspection 916478 of Aesculap Implant Systems LLC, March 04, 2015. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 916478
- Company Name: Aesculap Implant Systems LLC
- Inspection Date: 2015-03-04
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1223353 - 2023-11-09
- [FDA Inspection 1143458 - 2021-06-08](https://www.keypedia.com/records/fda_inspections/aesculap-implant-systems-llc/a9561303-ed9e-4bc3-9b0c-8da6c5f92868)
- FDA Inspection 796358 - 2012-08-27

Company: https://www.keypedia.com/companies/aesculap-implant-systems-llc/f8c60868-dbdf-4e2b-9bd7-5e5b4ff046ee

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7