FDA Inspection 934706 — DUSA Pharmaceuticals, Inc.

DUSA Pharmaceuticals, Inc. — FEI 3002513708

The FDA completed an inspection of DUSA Pharmaceuticals, Inc. on May 29, 2015 in Billerica, 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
May 29, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Billerica, MA (United States)