FDA inspection
QualTech Laboratories, Inc.: FDA inspection ending May 30, 2008
FDA inspection 521351 · No Action Indicated (NAI) · Ocean, NJ
Key facts
| Inspection ID | 521351 |
|---|---|
| Firm | QualTech Laboratories, Inc. |
| FEI number | 3000209713 |
| Address | 104 Green Grove Rd |
| City | Ocean |
| State | NJ |
| ZIP | 07712-3103 |
| Fiscal year | 2008 |
| Inspection end date | May 30, 2008 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | 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