Orca1

FDA inspection

Breg Inc: FDA inspection ending Aug 6, 2003

FDA inspection 286110 · Voluntary Action Indicated (VAI) · Carlsbad, CA

Key facts

Inspection ID 286110
Firm Breg Inc
FEI number 1000125378
Address 2885 Loker Ave E
City Carlsbad
State CA
ZIP 92010-6626
Fiscal year 2003
Inspection end date Aug 6, 2003
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|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 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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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