FDA inspection
Sunrider Manufacturing L P: FDA inspection ending Jul 11, 2008
FDA inspection 544226 · Midlothian, TX
Key facts
| Inspection ID | 544226 |
|---|---|
| Firm | Sunrider Manufacturing L P |
| FEI number | 1000125398 |
| Address | 3201 Challenger Dr |
| City | Midlothian |
| State | TX |
| ZIP | 76065 |
| Fiscal year | 2008 |
| Inspection end date | Jul 11, 2008 |
| 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