FDA inspection

Penn Pharmaceutical Services Ltd.: FDA inspection ending Jun 1, 2007

FDA inspection 477086 · Voluntary Action Indicated (VAI) · Tredegar

Key facts

Inspection ID 477086
Firm Penn Pharmaceutical Services Ltd.
FEI number 1000370240
Address Unit 23-24, Tafarnaubach Industrial Estate
City Tredegar
Fiscal year 2007
Inspection end date Jun 1, 2007
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 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|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

  • 1–9 Citations
  • 1–9 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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