FDA inspection

DUSA Pharmaceuticals, Inc.: FDA inspection ending Jun 13, 2007

FDA inspection 477141 · No Action Indicated (NAI) · Wilmington, MA

Key facts

Inspection ID 477141
Firm DUSA Pharmaceuticals, Inc.
FEI number 3002513708
Address 25 Upton Dr
City Wilmington
State MA
ZIP 01887-4409
Fiscal year 2007
Inspection end date Jun 13, 2007
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Drug 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Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices
Product type Devices, Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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