FDA inspection
RAPID RELEASE TECHNOLOGIES: FDA inspection ending May 25, 2016
FDA inspection 977555 · Official Action Indicated (OAI) · Costa Mesa, CA
Key facts
| Inspection ID | 977555 |
|---|---|
| Firm | RAPID RELEASE TECHNOLOGIES |
| FEI number | 3009341046 |
| Address | 3621 W Macarthur Blvd Ste 111 |
| City | Costa Mesa |
| State | CA |
| ZIP | 92626 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | May 25, 2016 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 507144 |
At a glance
- 1–9 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