FDA inspection
Dura Medical Equipment Dba Bay Shore Dura Medical: FDA inspection ending Jan 26, 2000
FDA inspection 11899 · Voluntary Action Indicated (VAI) · Miami Lakes, FL
Key facts
| Inspection ID | 11899 |
|---|---|
| Firm | Dura Medical Equipment Dba Bay Shore Dura Medical |
| FEI number | 1000143687 |
| Address | 7835 NW 148th St |
| City | Miami Lakes |
| State | FL |
| ZIP | 33016-1554 |
| Fiscal year | 2000 |
| Inspection end date | Jan 26, 2000 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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