FDA inspection
DDC Technologies Inc.: FDA inspection ending Feb 11, 2003
FDA inspection 256569 · Voluntary Action Indicated (VAI) · Oceanside, NY
Key facts
| Inspection ID | 256569 |
|---|---|
| Firm | DDC Technologies Inc. |
| FEI number | 3002757272 |
| Address | 311 Woods Ave |
| City | Oceanside |
| State | NY |
| ZIP | 11572-2128 |
| Fiscal year | 2003 |
| Inspection end date | Feb 11, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med 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
- 10–99 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