FDA Inspection 1089783 — Novaprobe Inc.

Novaprobe Inc. — FEI 3010120217

The FDA completed an inspection of Novaprobe Inc. on April 15, 2019 in Lansdale, PA. 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
April 15, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Lansdale, PA (United States)