FDA inspection
DDC Technologies, Inc.: FDA inspection ending Nov 9, 2015
FDA inspection 948368 · Voluntary Action Indicated (VAI) · Oceanside, NY
Key facts
| Inspection ID | 948368 |
|---|---|
| Firm | DDC Technologies, Inc. |
| FEI number | 3002757272 |
| Address | 311 Woods Ave |
| City | Oceanside |
| State | NY |
| ZIP | 11572 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Nov 9, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 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