# FDA Inspection 828602 - Aesculap Inc - April 24, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/aesculap-inc/2709437a-c7bf-4a97-a1b0-d7273810719c
Source feed: FDA_Inspections

> FDA Inspection 828602 for Aesculap Inc on April 24, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 828602
- Company Name: Aesculap Inc
- Inspection Date: 2013-04-24
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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