FDA Inspection 1267578 — BioAccess, Inc.

BioAccess, Inc. — FEI 1000513050

The FDA completed an inspection of BioAccess, Inc. on April 22, 2025 in Baltimore, MD. 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
April 22, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Baltimore, MD (United States)

Citations

IDCFRDescription
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures