FDA Inspection 993631 — BioAccess, Inc.

BioAccess, Inc. — FEI 1000513050

The FDA completed an inspection of BioAccess, Inc. on November 17, 2016 in Baltimore, MD. 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
November 17, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Baltimore, MD (United States)