# Caerus Corp. dba Orthocor Medical - Inspection Records

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

> Inspection records and compliance data for Caerus Corp. dba Orthocor Medical in Blaine, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: Caerus Corp. dba Orthocor Medical
- FEI Number: 3008216220
- City: Blaine
- State: Minnesota
- Country Name: United States
- Address Line 1: 8611 W 35w Service Dr Ne Suite 180
- Zip Code: 55449

## Related Documents

- [FDA Inspection 1305244 - Caerus Corp. dba Orthocor Medical - 2026-02-27](https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/be032d1a-fdbd-4ea4-bd99-738aefad77ce) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 27, 2026
- [FDA Inspection 1305244 - Caerus Corp. dba Orthocor Medical - 2026-02-27](https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/a5fadb75-3f85-4e60-836d-3e4d73f6a66e) — classification: No Action Indicated (NAI), source: FDA, date: February 27, 2026
- [FDA Inspection 1305244 - Caerus Corp. dba Orthocor Medical - 2026-02-27](https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/82e4c53b-d335-4a3b-b54b-b9176ba5d0d0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 27, 2026
- [FDA Inspection 1305244 - Caerus Corp. dba Orthocor Medical - 2026-02-27](https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/3064d565-2727-4731-b425-38704067d6bf) — classification: No Action Indicated (NAI), source: FDA, date: February 27, 2026
- [483 - Caerus Corp. dba Orthocor Medical - 2022-11-22](https://www.globalkeysolutions.net/records/483/caerus-corp-dba-orthocor-medical/24cef1ee-6b39-4291-bc88-1e137d5a9f22) — source: FDA, date: November 22, 2022
- [FDA Inspection 1191173 - Caerus Corp. dba Orthocor Medical - 2022-11-22](https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/6bb5400f-ea90-4173-96d5-eda72316218d) — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2022
- [FDA Inspection 1191173 - Caerus Corp. dba Orthocor Medical - 2022-11-22](https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/53072c9f-8420-4a38-bee3-32e64ce48145) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 22, 2022
- [483 - Caerus Corp. dba Orthocor Medical - 2019-04-24](https://www.globalkeysolutions.net/records/483/caerus-corp-dba-orthocor-medical/b1d0f574-14ec-4959-9c67-ebb8a0f6b442) — source: FDA, date: April 24, 2019
- [FDA Inspection 1088096 - Caerus Corp. dba Orthocor Medical - 2019-04-24](https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/20a4b3d4-4589-4352-9791-615eccc56efa) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 24, 2019
- [FDA Inspection 1088096 - Caerus Corp. dba Orthocor Medical - 2019-04-24](https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/5683e9ee-279a-4055-b2d5-96794de44cdc) — classification: No Action Indicated (NAI), source: FDA, date: April 24, 2019
- [FDA Inspection 1072151 - Caerus Corp. dba Orthocor Medical - 2018-10-10](https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/1b835779-91b1-4c73-a398-c0aad0d46a53) — classification: No Action Indicated (NAI), source: FDA, date: October 10, 2018
- [FDA Inspection 946141 - Caerus Corp. dba Orthocor Medical - 2015-09-09](https://www.globalkeysolutions.net/records/fda_inspections/caerus-corp-dba-orthocor-medical/634b994a-2dd8-489d-857a-37676ab3583a) — classification: No Action Indicated (NAI), source: FDA, date: September 9, 2015

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