FDA Inspection 1217179 — DUSA Pharmaceuticals, Inc.

DUSA Pharmaceuticals, Inc. — FEI 3002513708

The FDA completed an inspection of DUSA Pharmaceuticals, Inc. on September 8, 2023 in Billerica, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 8, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Billerica, MA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures