# FDA 483 - Multi-Med, Inc. - September 19, 2024

Source: https://www.keypedia.com/records/483/multi-med-inc/161d8f7a-646e-4746-b54b-0db713ba3242

> FDA 483 for Multi-Med, Inc. on September 19, 2024. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Multi-Med, Inc.
- Inspection Date: 2024-09-19
- Product Type: device
- Office Name: New England District Office
- Summary: An FDA inspection of Multi-Med, Inc. in Keene, NH, a medical device manufacturer, revealed three significant observations. The firm was cited for inadequate documentation of labels and labeling, including expiration dates for sterile devices, and insufficient records for in-house equipment calibrations. Additionally, deficiencies were noted in the maintenance of device history records, specifically regarding sterilization process documentation.

## Related Officers

- [investigator](https://www.keypedia.com/people/kwong-p-lee/f4778925-1fad-4988-9e39-86482896c4fa)

Company: https://www.keypedia.com/companies/multi-med-inc/f76d7a4d-2ec1-4035-b7e1-3d615619a705

Office: https://www.keypedia.com/offices/new-england-district-office/aa458072-2f1d-4231-89f5-21ba7a3b7144