# FDA Inspection 1088096 - Caerus Corp. dba Orthocor Medical - April 24, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/5683e9ee-279a-4055-b2d5-96794de44cdc
Source feed: FDA_Inspections

> FDA Inspection 1088096 for Caerus Corp. dba Orthocor Medical on April 24, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1088096
- Company Name: Caerus Corp. dba Orthocor Medical
- Inspection Date: 2019-04-24
- 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/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