FDA inspection
ORTHO PRECISION PRODUCTS: FDA inspection ending Jun 8, 2016
FDA inspection 978371 · Voluntary Action Indicated (VAI) · Hawthorne, CA
Key facts
| Inspection ID | 978371 |
|---|---|
| Firm | ORTHO PRECISION PRODUCTS |
| FEI number | 3011053036 |
| Address | 3201 W El Segundo Blvd |
| City | Hawthorne |
| State | CA |
| ZIP | 90250-4814 |
| Fiscal year | 2016 |
| Inspection end date | Jun 8, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
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