FDA inspection
Scientech Laboratories Inc: FDA inspection ending Oct 31, 2001
FDA inspection 126182 · Voluntary Action Indicated (VAI) · S Plainfield, NJ
Key facts
| Inspection ID | 126182 |
|---|---|
| Firm | Scientech Laboratories Inc |
| FEI number | 2243943 |
| Address | 107G Corporate Blvd |
| City | S Plainfield |
| State | NJ |
| ZIP | 07080-2454 |
| Fiscal year | 2002 |
| Inspection end date | Oct 31, 2001 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug 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Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug Evaluation|Monit of Marketed Animal Drug,Feed &Dev|Generic Drug 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| Product type | 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.
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