# FDA Inspection 1305244 - Caerus Corp. dba Orthocor Medical - February 27, 2026

Source: https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/3064d565-2727-4731-b425-38704067d6bf
Source feed: FDA_Inspections

> FDA Inspection 1305244 for Caerus Corp. dba Orthocor Medical on February 27, 2026. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1305244
- Company Name: Caerus Corp. dba Orthocor Medical
- Inspection Date: 2026-02-27
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices

## Related Documents

- [FDA Inspection 1305244 - 2026-02-27](https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/a5fadb75-3f85-4e60-836d-3e4d73f6a66e)
- [FDA Inspection 1305244 - 2026-02-27](https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/be032d1a-fdbd-4ea4-bd99-738aefad77ce)
- [FDA Inspection 1305244 - 2026-02-27](https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/82e4c53b-d335-4a3b-b54b-b9176ba5d0d0)
- [FDA Inspection 1191173 - 2022-11-22](https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/53072c9f-8420-4a38-bee3-32e64ce48145)
- [FDA Inspection 1191173 - 2022-11-22](https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/6bb5400f-ea90-4173-96d5-eda72316218d)

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