# dBMEDx, Inc - Inspection Records

Source: https://www.globalkeysolutions.net/companies/dbmedx-inc/82780a51-aeff-400d-90ca-40e73b2c7e11

> Inspection records and compliance data for dBMEDx, Inc in Littleton, Colorado. Access full analysis and detailed observations.

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## Details

- Name: dBMEDx, Inc
- FEI Number: 3008321254
- City: Littleton
- State: Colorado
- Country Name: United States
- Address Line 1: 7761 Shaffer Pkwy Ste 140
- Zip Code: 80127

## Related Documents

- [483 - dBMEDx, Inc - 2025-03-27](https://www.globalkeysolutions.net/records/483/dbmedx-inc/b55df468-1e40-4394-858a-d0e728362286) — source: FDA, date: March 27, 2025
- [FDA Inspection 1265088 - dBMEDx, Inc - 2025-03-27](https://www.globalkeysolutions.net/records/fda_inspections/dbmedx-inc/b0cf38ea-1e5a-48bb-9720-78dd44b2a2ca) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 27, 2025
- [FDA Inspection 1265088 - dBMEDx, Inc - 2025-03-27](https://www.globalkeysolutions.net/records/fda_inspections/dbmedx-inc/1d483c79-271f-4921-9fd3-3ba9fe7349ba) — classification: No Action Indicated (NAI), source: FDA, date: March 27, 2025
- [FDA Inspection 1265088 - dBMEDx, Inc - 2025-03-27](https://www.globalkeysolutions.net/records/fda_inspections/dbmedx-inc/82e83557-8cf8-47a7-83be-3da8c7074b6e) — classification: No Action Indicated (NAI), source: FDA, date: March 27, 2025
- [FDA Inspection 1265088 - dBMEDx, Inc - 2025-03-27](https://www.globalkeysolutions.net/records/fda_inspections/dbmedx-inc/45d064ee-455d-4cf9-9895-48efcd066b1e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 27, 2025
- [FDA Inspection 989535 - dBMEDx, Inc - 2016-10-07](https://www.globalkeysolutions.net/records/fda_inspections/dbmedx-inc/0a27b557-13e8-4a2e-995e-ccffee1fd89a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 7, 2016
- [FDA Inspection 989535 - dBMEDx, Inc - 2016-10-07](https://www.globalkeysolutions.net/records/fda_inspections/dbmedx-inc/685dc4cc-c554-425e-b5de-e74fbc2a2f1f) — classification: No Action Indicated (NAI), source: FDA, date: October 7, 2016

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