Orca1

FDA inspection

Lee Medical International, Inc.: FDA inspection ending Mar 14, 2005

FDA inspection 364865 · Official Action Indicated (OAI) · Harahan, LA

Key facts

Inspection ID 364865
Firm Lee Medical International, Inc.
FEI number 2316883
Address 612 Distributors Row
City Harahan
State LA
ZIP 70123-3206
Fiscal year 2005
Inspection end date Mar 14, 2005
Classification Official Action Indicated (OAI)
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|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: 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Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices|Drug Quality Assurance|Postmarket Assurance: Med Devices
Product type Devices, Drugs
Warning letter UCM075457

At a glance

  • 10–99 Citations
  • 1–9 Posted citations
  • Yes 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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