FDA inspection
Winchester Laboratories, LLC: FDA inspection ending Jun 13, 2017
FDA inspection 1014220 · Voluntary Action Indicated (VAI) · Delray Beach, FL
Key facts
| Inspection ID | 1014220 |
|---|---|
| Firm | Winchester Laboratories, LLC |
| FEI number | 3003036307 |
| Address | 301 W Atlantic Ave Ste 1 |
| City | Delray Beach |
| State | FL |
| ZIP | 33444 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Jun 13, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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
- 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