FDA inspection
Element Materials Technology Pharma US LLC: FDA inspection ending May 3, 2019
FDA inspection 1088621 · Voluntary Action Indicated (VAI) · Santa Fe Springs, CA
Key facts
| Inspection ID | 1088621 |
|---|---|
| Firm | Element Materials Technology Pharma US LLC |
| FEI number | 3000203007 |
| Address | 9240 Santa Fe Springs Rd |
| City | Santa Fe Springs |
| State | CA |
| ZIP | 90670 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | May 3, 2019 |
| 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
- Yes 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