# FDA 483 - Retmap Inc - October 30, 2025

Source: https://www.globalkeysolutions.net/records/483/retmap-inc/58ebb169-777e-4508-bbd9-d0c470f388be

> FDA 483 for Retmap Inc on October 30, 2025. Product: other. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Retmap Inc
- Inspection Date: 2025-10-30
- Product Type: other
- Office Name: Chicago District Office
- Summary: An FDA inspection of Retmap Inc, a manufacturer in Chicago, revealed significant deficiencies across its quality system. Observations included inadequate documentation of equipment maintenance, failure to control nonconforming products, and insufficient supplier management. The firm also lacked proper procedures for corrective and preventive actions, failed to conduct timely management reviews, and did not perform required quality audits.

## Related Officers

- [Medical Device Specialist](https://www.globalkeysolutions.net/people/jesse-a-vazquez/cac5b170-d0ea-4355-af5d-3d81546ff0fe)

Company: https://www.globalkeysolutions.net/companies/retmap-inc/40163943-157c-482c-926d-f72cbaa49246

Office: https://www.globalkeysolutions.net/offices/chicago-district-office/a510300b-0eaf-4a33-90b5-231d95977669