# FDA 483 - Caerus Corp. dba Orthocor Medical - April 24, 2019

Source: https://www.keypedia.com/records/483/caerus-corp-dba-orthocor-medical/b1d0f574-14ec-4959-9c67-ebb8a0f6b442

> FDA 483 for Caerus Corp. dba Orthocor Medical on April 24, 2019. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Caerus Corp. dba Orthocor Medical
- Inspection Date: 2019-04-24
- Product Type: device
- Office Name: Minneapolis District Office
- Summary: Caerus Corp. dba Orthocor Medical, a medical device manufacturer in Arden Hills, MN, was inspected and cited for inadequate complaint handling procedures. The firm failed to timely initiate complaint records, conduct and document complete investigations, and adequately assess complaints for Medical Device Report (MDR) reportability.

## Related Documents

- [483 - 2022-11-22](https://www.keypedia.com/records/483/caerus-corp-dba-orthocor-medical/24cef1ee-6b39-4291-bc88-1e137d5a9f22)

## Related Officers

- [investigator](https://www.keypedia.com/people/jennifer-s-ness/532f8a81-e393-4e83-b5f2-a72362e966de)

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

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d