FDA Inspection 720086 — Accumin Diagnostics, Inc.

Accumin Diagnostics, Inc. — FEI 3005609175

The FDA completed an inspection of Accumin Diagnostics, Inc. on March 3, 2011 in New York, NY. 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
March 3, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
New York, NY (United States)