FDA inspection
Kenlor Industries, Inc.: FDA inspection ending May 3, 2019
FDA inspection 1088389 · Official Action Indicated (OAI) · Santa Ana, CA
Key facts
| Inspection ID | 1088389 |
|---|---|
| Firm | Kenlor Industries, Inc. |
| FEI number | 2027370 |
| Address | 1560 E Edinger Ave Ste A1 |
| City | Santa Ana |
| State | CA |
| ZIP | 92705 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | May 3, 2019 |
| Classification | Official Action Indicated (OAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- 10–99 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