Orca1

FDA inspection

Harry J Bosworth Company: FDA inspection ending Dec 22, 2004

FDA inspection 361324 · Official Action Indicated (OAI) · Skokie, IL

Key facts

Inspection ID 361324
Firm Harry J Bosworth Company
FEI number 1410638
Address 7227 Hamlin Ave
City Skokie
State IL
ZIP 60076-3901
Fiscal year 2005
Inspection end date Dec 22, 2004
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

At a glance

  • 10–99 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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