FDA Inspection 1316152 — SPIRAIR, INC.

SPIRAIR, INC. — FEI 3030653921

The FDA completed an inspection of SPIRAIR, INC. on May 1, 2026 in South San Francisco, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 1, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
South San Francisco, CA (United States)