# FDA Inspection 1289902 - Retmap Inc - October 30, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/retmap-inc/aa53b33e-c9f8-4422-a516-77bcdf96a617
Source feed: FDA_Inspections

> FDA Inspection 1289902 for Retmap Inc on October 30, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1289902
- Company Name: Retmap Inc
- Inspection Date: 2025-10-30
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Chicago District Office

## Related Documents

- [FDA Inspection 1289902 - 2025-10-30](https://www.globalkeysolutions.net/records/fda_inspections/retmap-inc/0aefaa42-48f3-4536-aff8-952e788f8a19)
- [FDA Inspection 1289902 - 2025-10-30](https://www.globalkeysolutions.net/records/fda_inspections/retmap-inc/e4d54eee-fb8d-406f-a460-a51592d9603b)
- [FDA Inspection 1289902 - 2025-10-30](https://www.globalkeysolutions.net/records/fda_inspections/retmap-inc/f857a39f-98d2-409b-858f-f32da9b3c78f)

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