# BOULDER BIOMED DBA BOULDER IQ – FDA Inspection, Oct 30, 2023

Source: https://www.keypedia.com/records/fda_inspections/boulder-biomed-dba-boulder-iq/3c241418-4c1a-4584-9800-ae6472ca9df9
Source feed: FDA_Inspections

> FDA inspection 1221441 of BOULDER BIOMED DBA BOULDER IQ, October 30, 2023. Classification: No Action Indicated (NAI). 5 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1221441
- Company Name: BOULDER BIOMED DBA BOULDER IQ
- Inspection Date: 2023-10-30
- 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: 5

## Related Officers

- [Company Rep](https://www.keypedia.com/people/christine-i-shaw/480cb61e-f173-432d-b84a-c8b492192302)

Company: https://www.keypedia.com/companies/boulder-biomed-dba-boulder-iq/85c6f76e-a457-4ec2-bce3-a2276bc09484

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