# FDA Inspection 1072151 - Caerus Corp. dba Orthocor Medical - October 10, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/1b835779-91b1-4c73-a398-c0aad0d46a53
Source feed: FDA_Inspections

> FDA Inspection 1072151 for Caerus Corp. dba Orthocor Medical on October 10, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1072151
- Company Name: Caerus Corp. dba Orthocor Medical
- Inspection Date: 2018-10-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/caerus-corp-dba-orthocor-medical/5bbb3b68-b24e-42b4-b35d-5aae22299e2c

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