FDA inspection
Asclemed USA Inc.: FDA inspection ending Sep 27, 2018
FDA inspection 1067059 · Official Action Indicated (OAI) · Torrance, CA
Key facts
| Inspection ID | 1067059 |
|---|---|
| Firm | Asclemed USA Inc. |
| FEI number | 3001452204 |
| Address | 379 Van Ness Ave Ste 1403 |
| City | Torrance |
| State | CA |
| ZIP | 90501 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Sep 27, 2018 |
| Classification | Official Action Indicated (OAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
| Warning letter | 575542 |
At a glance
- None Citations
- 1–9 Posted citations
- Yes 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