There was one company in a city associated with Ingham County that received FDA citations as a result of one inspection conducted in the county over the second quarter of 2025, according to reports from the U.S. Food and Drug Administration (FDA).
This is an increase over the number of companies cited in the previous quarter.
The citations in the county include:
- Procedures for design change have not been adequately established.
- Procedures to ensure that all purchased or otherwise received product and services conform to specified requirements have not been adequately established.
- Procedures for identifying product during all stages of receipt, production, distribution, and installation have not been adequately established.
The company cited was involved in the Devices sector.
The company cited should take a voluntary action to correct its managing operations.
The FDA routinely inspects facilities across the nation to determine if the workplace and their products are compliant with FDA-regulated laws and regulations implemented to improve overall public health. Inspection results are then disclosed publicly.
According to its website, the FDA is a government agency that is primarily responsible for monitoring the production and distribution of human and animal drugs, biological products, medical supplies and tobacco products for safety quality.
| Company Name | Area of Business | Inspection Date | Issue Cited |
|---|---|---|---|
| Neogen Culture Media | Devices | 04/07/2025 | Design changes – Lack of or Inadequate Procedures |
| Neogen Culture Media | Devices | 04/07/2025 | Purchasing controls, Lack of or inadequate procedures |
| Neogen Culture Media | Devices | 04/07/2025 | Identification procedures, Lack of or inadequate procedures |
| Neogen Culture Media | Devices | 04/07/2025 | Lack/Inad procedure-Monitoring/Control of Validated Proces |
| Neogen Culture Media | Devices | 04/07/2025 | Lack of or inadequate procedures |
| Neogen Culture Media | Devices | 04/07/2025 | DMR – not or inadequately maintained |
| Neogen Culture Media | Devices | 04/07/2025 | Lack of or inadequate DHR procedures |
| Neogen Culture Media | Devices | 04/07/2025 | Investigation of device failures |
