# FDA 483 - Symmetry Medical Manufacturing, Inc. - October 21, 2022

Source: https://www.keypedia.com/records/483/symmetry-medical-manufacturing-inc/f7861059-ebbe-4ac2-a274-218714902313

> FDA 483 for Symmetry Medical Manufacturing, Inc. on October 21, 2022. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Symmetry Medical Manufacturing, Inc.
- Inspection Date: 2022-10-21
- Product Type: device
- Office Name: Division of Northeast Imports 
- Summary: Symmetry Medical Manufacturing, Inc., a medical device manufacturer in Manchester, NH, was issued a Form FDA 483 following an inspection from October 13-21, 2022. The inspection revealed a significant deficiency in the firm's corrective and preventive action procedures, specifically regarding the failure to address systemic document control issues identified in multiple internal reports. This indicates a breakdown in the quality system's ability to manage and control essential documentation.

## Related Officers

- [CSO at FDA](https://www.keypedia.com/people/justine-m-corson/5f6e4477-f060-47f1-9165-a63fd6a36226)

Company: https://www.keypedia.com/companies/symmetry-medical-manufacturing-inc/efc7ce73-1c6b-4611-bff0-d14b9c9b2c2c

Office: https://www.keypedia.com/offices/division-of-northeast-imports/b20599cf-9797-41fd-947f-6589ef596a94