FDA Inspection 1273673 — Freespira, Inc.

Freespira, Inc. — FEI 3010887638

The FDA completed an inspection of Freespira, Inc. on Jun 16, 2025 in Kirkland, WA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 16, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Kirkland, WA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures

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