FDA inspection
Pro-Tech Design & Manufacturing, Inc.: FDA inspection ending Jul 27, 2016
FDA inspection 989126 · No Action Indicated (NAI) · Santa Fe Springs, CA
Key facts
| Inspection ID | 989126 |
|---|---|
| Firm | Pro-Tech Design & Manufacturing, Inc. |
| FEI number | 3003574398 |
| Address | 14561 Marquardt Ave |
| City | Santa Fe Springs |
| State | CA |
| ZIP | 90670 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Jul 27, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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