FDA inspection
Catalent CTS, LLC: FDA inspection ending Mar 23, 2026
FDA inspection 1313380 · Kansas City, MO
Key facts
| Inspection ID | 1313380 |
|---|---|
| Firm | Catalent CTS, LLC |
| FEI number | 3002929455 |
| Address | 10245 Hickman Mills Dr |
| City | Kansas City |
| State | MO |
| ZIP | 64137-1418 |
| Fiscal year | 2026 |
| Inspection end date | Mar 23, 2026 |
| Project area | Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices|Monitoring of Marketed Animal Drugs, Feeds, and Devices |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 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