# dBMEDx, Inc – FDA Inspection, Oct 7, 2016

Source: https://www.keypedia.com/records/fda_inspections/dbmedx-inc/685dc4cc-c554-425e-b5de-e74fbc2a2f1f
Source feed: FDA_Inspections

> FDA inspection 989535 of dBMEDx, Inc, October 07, 2016. Classification: No Action Indicated (NAI). 4 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 989535
- Company Name: dBMEDx, Inc
- Inspection Date: 2016-10-07
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1265088 - 2025-03-27](https://www.keypedia.com/records/fda_inspections/dbmedx-inc/1d483c79-271f-4921-9fd3-3ba9fe7349ba)

## Related Officers

- [Investigator](https://www.keypedia.com/people/kathleen-s-tormey/5e1abfe2-078a-4c61-bb98-3885f853a945)

Company: https://www.keypedia.com/companies/dbmedx-inc/82780a51-aeff-400d-90ca-40e73b2c7e11

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7