FDA inspection
CorePharma, LLC: FDA inspection ending Aug 31, 2021
FDA inspection 1153831 · No Action Indicated (NAI) · Middlesex, NJ
Key facts
| Inspection ID | 1153831 |
|---|---|
| Firm | CorePharma, LLC |
| FEI number | 3002535019 |
| Address | 215 Wood Ave |
| City | Middlesex |
| State | NJ |
| ZIP | 08846-2554 |
| Fiscal year | 2021 |
| Inspection end date | Aug 31, 2021 |
| Classification | No Action Indicated (NAI) |
| Project area | Generic Drug Evaluation |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 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