FDA inspection
Anholt Technologies, Inc.: FDA inspection ending Sep 24, 2018
FDA inspection 1069651 · No Action Indicated (NAI) · Avondale, PA
Key facts
| Inspection ID | 1069651 |
|---|---|
| Firm | Anholt Technologies, Inc. |
| FEI number | 1000208827 |
| Address | 440 Church Rd |
| City | Avondale |
| State | PA |
| ZIP | 19311 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Sep 24, 2018 |
| Classification | No Action Indicated (NAI) |
| Project area | Radiation Control and Health Safety Act |
| 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