FDA inspection
R & D Medical Products, Inc.: FDA inspection ending Jul 14, 2016
FDA inspection 977940 · Voluntary Action Indicated (VAI) · Lake Forest, CA
Key facts
| Inspection ID | 977940 |
|---|---|
| Firm | R & D Medical Products, Inc. |
| FEI number | 3001236548 |
| Address | 20492 Crescent Bay Dr Ste 106 |
| City | Lake Forest |
| State | CA |
| ZIP | 92630 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Jul 14, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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