FDA Inspection 1231451 — Glooko, Inc

Glooko, Inc — FEI 3009137498

The FDA completed an inspection of Glooko, Inc on Feb 1, 2024 in Palo Alto, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 1, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Palo Alto, CA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.