Orca1

FDA inspection

Mayne Pharma (PR) Inc.: FDA inspection ending Apr 3, 2000

FDA inspection 19878 · Voluntary Action Indicated (VAI) · Aguadilla, PR

Key facts

Inspection ID 19878
Firm Mayne Pharma (PR) Inc.
FEI number 2650040
Address 1071 Parallel Rd., Ramey
City Aguadilla
State PR
ZIP 00604
Fiscal year 2000
Inspection end date Apr 3, 2000
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic 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Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug Evaluation|Product Evaluation: Med Devices|Generic Drug 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Product type Devices, Drugs

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

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

Other inspections at this establishment

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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