# FDA Inspection 1221441 - BOULDER BIOMED DBA BOULDER IQ - October 30, 2023

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

> FDA Inspection 1221441 for BOULDER BIOMED DBA BOULDER IQ on October 30, 2023. Classification: No Action Indicated (NAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1221441 - 2023-10-30](https://www.globalkeysolutions.net/records/fda_inspections/boulder-biomed-dba-boulder-iq/075d4e38-e676-4cd0-8624-9e869ebc0aba)

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

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