FDA inspection
GlaxoSmithKline LLC: FDA inspection ending Apr 21, 2016
FDA inspection 987392 · Voluntary Action Indicated (VAI) · Zebulon, NC
Key facts
| Inspection ID | 987392 |
|---|---|
| Firm | GlaxoSmithKline LLC |
| FEI number | 1033964 |
| Address | 1011 N Arendell Ave |
| City | Zebulon |
| State | NC |
| ZIP | 27597 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Apr 21, 2016 |
| 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
- 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