FDA Inspection 1318370 — Biofilm, Inc.

Biofilm, Inc. — FEI 2025771

The FDA completed an inspection of Biofilm, Inc. on May 19, 2026 in Vista, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 19, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Vista, CA (United States)

Citations

IDCFRDescription
73121 CFR 803.50(a)(1)Report of Death or Serious Injury