FDA inspection

Horizon Pharmaceuticals, Inc.: FDA inspection ending Jan 14, 2000

FDA inspection 10354 · Voluntary Action Indicated (VAI) · Palm Beach Gardens, FL

Key facts

Inspection ID 10354
Firm Horizon Pharmaceuticals, Inc.
FEI number 3000718824
Address 10180 Riverside Dr
City Palm Beach Gardens
State FL
ZIP 33410-4880
Fiscal year 2000
Inspection end date Jan 14, 2000
Classification Voluntary Action Indicated (VAI)
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|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med 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Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices
Product type Devices, Drugs

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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