There was one company in a city associated with Cheshire County that received FDA citations as a result of one inspection conducted in the county in September, 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 month.
The citations in the county include:
- Equipment calibrations have not been documented.
- Labels and labeling used for each finished product, lot, or batch, were not sufficiently documented in the DHR.
- A device history record has not been adequately maintained.
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.
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, according to its website.
| Company Name | Area of Business | Inspection Date | Issue Cited |
|---|---|---|---|
| Multi-Med, Inc. | Devices | 09/19/2024 | Equipment control activity documentation |
| Multi-Med, Inc. | Devices | 09/19/2024 | Records, DHR {see also 820.184(e)} |
| Multi-Med, Inc. | Devices | 09/19/2024 | DHR – not or inadequately maintained |
