FDA inspection
Nelson Laboratories LLC: FDA inspection ending Aug 18, 2005
FDA inspection 393226 · No Action Indicated (NAI) · Itasca, IL
Key facts
| Inspection ID | 393226 |
|---|---|
| Firm | Nelson Laboratories LLC |
| FEI number | 3000717698 |
| Address | 1500 W Thorndale Ave |
| City | Itasca |
| State | IL |
| ZIP | 60143-1133 |
| Fiscal year | 2005 |
| Inspection end date | Aug 18, 2005 |
| Classification | No Action Indicated (NAI) |
| 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 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Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices|Drug Quality Assurance|Monit of Marketed Animal Drug,Feed &Dev|Product Evaluation: Med Devices |
| Product type | Devices, Drugs |
At a glance
- None Citations
- None 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.
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