FDA Inspection 1316010 — Capnia, Inc.

Capnia, Inc. — FEI 3008614998

The FDA completed an inspection of Capnia, Inc. on May 7, 2026 in Foster City, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 7, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Foster City, CA (United States)