FDA Inspection 577342 — Pulpdent Corporation

Pulpdent Corporation — FEI 1215305

The FDA completed an inspection of Pulpdent Corporation on April 17, 2009 in Watertown, MA. 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 17, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Watertown, MA (United States)