FDA inspection
INSYS MANUFACTURING, LLC: FDA inspection ending Dec 14, 2015
FDA inspection 953770 · Voluntary Action Indicated (VAI) · Round Rock, TX
Key facts
| Inspection ID | 953770 |
|---|---|
| Firm | INSYS MANUFACTURING, LLC |
| FEI number | 3009085408 |
| Address | 811 Paloma Dr Ste C |
| City | Round Rock |
| State | TX |
| ZIP | 78665 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Dec 14, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| 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
- 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