FDA inspection
ALS Group USA, Corp: FDA inspection ending Jun 18, 2014
FDA inspection 883899 · No Action Indicated (NAI) · Torrance, CA
Key facts
| Inspection ID | 883899 |
|---|---|
| Firm | ALS Group USA, Corp |
| FEI number | 2027219 |
| Address | 3904 Del Amo Blvd Ste 801 |
| City | Torrance |
| State | CA |
| ZIP | 90503 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Jun 18, 2014 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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