FDA Inspection 967762 — Nephros, Inc.

Nephros, Inc. — FEI 3003337893

The FDA completed an inspection of Nephros, Inc. on February 22, 2016 in Whippany, NJ. 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
February 22, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Whippany, NJ (United States)