# FDA Inspection 1231451 - Glooko, Inc - February 01, 2024

Source: https://www.keypedia.com/records/fda_inspections/glooko-inc/2ebc2417-dd4f-44c3-8bbe-1e5840d55b1e
Source feed: FDA_Inspections

> FDA Inspection 1231451 for Glooko, Inc on February 01, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1231451
- Company Name: Glooko, Inc
- Inspection Date: 2024-02-01
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1231451 - 2024-02-01](https://www.keypedia.com/records/fda_inspections/glooko-inc/15b0e82c-59a8-4637-897c-8b91cd9c98cc)

Company: https://www.keypedia.com/companies/glooko-inc/290837a0-66f4-44dd-b463-908612d14206

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