FDA Inspection 1316830 — Pulmonx, Corp.

Pulmonx, Corp. — FEI 3007797756

The FDA completed an inspection of Pulmonx, Corp. on Jul 2, 2026 in Redwood City, 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
Jul 2, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Redwood City, CA (United States)

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