FDA inspection
BAXTER HEALTHCARE CORPORATION: FDA inspection ending Mar 24, 2003
FDA inspection 256442 · Voluntary Action Indicated (VAI) · Round Lake, IL
Key facts
| Inspection ID | 256442 |
|---|---|
| Firm | BAXTER HEALTHCARE CORPORATION |
| FEI number | 1416980 |
| Address | 25212 W Il Route 120 |
| City | Round Lake |
| State | IL |
| ZIP | 60073-9799 |
| Fiscal year | 2003 |
| Inspection end date | Mar 24, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance|Blood and Blood Products|Compliance: Med Devices|Drug Quality Assurance |
| Product type | Biologics, Devices, Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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