FDA inspection
Novelart Manufacturing Inc.: FDA inspection ending Oct 16, 2025
FDA inspection 1287890 · No Action Indicated (NAI) · Cincinnati, OH
Key facts
| Inspection ID | 1287890 |
|---|---|
| Firm | Novelart Manufacturing Inc. |
| FEI number | 1513729 |
| Address | 2121 Section Rd |
| City | Cincinnati |
| State | OH |
| ZIP | 45237 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | Oct 16, 2025 |
| Classification | No Action Indicated (NAI) |
| Project area | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| Product type | Veterinary |
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