FDA inspection

Neogen Corporation: FDA inspection ending Mar 6, 2026

FDA inspection 1306238 · Lexington, KY

Key facts

Inspection ID 1306238
Firm Neogen Corporation
FEI number 3009631819
Address 1847 Mercer Rd Ste A
City Lexington
State KY
ZIP 40511-1001
Fiscal year 2026
Inspection end date Mar 6, 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

  • 1–9 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

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