FDA inspection

Mayne Pharma (PR) Inc.: FDA inspection ending Sep 28, 2001

FDA inspection 90080 · No Action Indicated (NAI) · Aguadilla, PR

Key facts

Inspection ID 90080
Firm Mayne Pharma (PR) Inc.
FEI number 2650040
Address 1071 Parallel Rd., Ramey
City Aguadilla
State PR
ZIP 00604
Fiscal year 2001
Inspection end date Sep 28, 2001
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|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug 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Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: 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
  • 1–9 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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