Orca1

FDA inspection

Boston Scientific Corp.: FDA inspection ending Jun 17, 2008

FDA inspection 526548 · Official Action Indicated (OAI) · Coventry, RI

Key facts

Inspection ID 526548
Firm Boston Scientific Corp.
FEI number 1000121056
Address 8 Industrial Dr
City Coventry
State RI
ZIP 02816-8927
Fiscal year 2008
Inspection end date Jun 17, 2008
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|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

  • None 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.

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

Browse all FDA inspections