FDA inspection
Medcraft Industries: FDA inspection ending Feb 15, 2000
FDA inspection 13839 · Official Action Indicated (OAI) · Bridgeport, CT
Key facts
| Inspection ID | 13839 |
|---|---|
| Firm | Medcraft Industries |
| FEI number | 1000220169 |
| Address | 1129 Howard Ave |
| City | Bridgeport |
| State | CT |
| ZIP | 06605-1615 |
| Fiscal year | 2000 |
| Inspection end date | Feb 15, 2000 |
| Classification | Official Action Indicated (OAI) |
| 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
- 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