FDA inspection
GlaxoSmithKline Consumer Healthcare, LP: FDA inspection ending Jul 11, 2008
FDA inspection 528359 · Voluntary Action Indicated (VAI) · Clifton, NJ
Key facts
| Inspection ID | 528359 |
|---|---|
| Firm | GlaxoSmithKline Consumer Healthcare, LP |
| FEI number | 2210777 |
| Address | 65 Industrial St S |
| City | Clifton |
| State | NJ |
| ZIP | 07012-1709 |
| Fiscal year | 2008 |
| Inspection end date | Jul 11, 2008 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 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