FDA inspection
Strides Pharma, Inc.: FDA inspection ending Dec 23, 2025
FDA inspection 1292202 · Chestnut Ridge, NY
Key facts
| Inspection ID | 1292202 |
|---|---|
| Firm | Strides Pharma, Inc. |
| FEI number | 2434223 |
| Address | 1 Ram Ridge Rd |
| City | Chestnut Ridge |
| State | NY |
| ZIP | 10977-6714 |
| Fiscal year | 2026 |
| Inspection end date | Dec 23, 2025 |
| Project area | Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices|Drug Quality Assurance|Postmarket Assurance: Medical Devices |
| Product type | Devices, 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