FDA inspection
Protech Professional Products, Inc.: FDA inspection ending Oct 28, 2016
FDA inspection 990471 · Voluntary Action Indicated (VAI) · Boynton Beach, FL
Key facts
| Inspection ID | 990471 |
|---|---|
| Firm | Protech Professional Products, Inc. |
| FEI number | 1000137415 |
| Address | 2900 Commerce Park Dr Ste 10 |
| City | Boynton Beach |
| State | FL |
| ZIP | 33426 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Oct 28, 2016 |
| 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