FDA inspection
Robertson Microlit Laboratories, Inc.: FDA inspection ending Jan 20, 2010
FDA inspection 638383 · No Action Indicated (NAI) · Ledgewood, NJ
Key facts
| Inspection ID | 638383 |
|---|---|
| Firm | Robertson Microlit Laboratories, Inc. |
| FEI number | 2246982 |
| Address | 1705 US Highway 46 Ste 1D |
| City | Ledgewood |
| State | NJ |
| ZIP | 07852 |
| Country | United States |
| Fiscal year | 2010 |
| Inspection end date | Jan 20, 2010 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| 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