# FDA 483 - MANCHESTER VA MEDICAL CENTER - January 27, 2020

Source: https://www.keypedia.com/records/483/manchester-va-medical-center/faf8b113-d035-4b07-840b-45f99c8f8e86

> FDA 483 for MANCHESTER VA MEDICAL CENTER on January 27, 2020. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: MANCHESTER VA MEDICAL CENTER
- Inspection Date: 2020-01-27
- Product Type: drugs
- Office Name: Division of Northeast Imports 
- Summary: The FDA inspected Manchester VA Medical Center, a producer of sterile and non-sterile drug products, and identified significant deficiencies. Observations included non-sterile cleaning agents and practices in aseptic processing areas, inadequate facility design leading to poor air quality, and insufficient environmental monitoring. These issues collectively indicate a lack of control over the manufacturing environment, posing risks to product quality and patient safety.

## Related Officers

- [Arizona Market President](https://www.keypedia.com/people/john-p-mistler/7b2d423d-46cc-48bd-aa5a-4ae794888060)

Company: https://www.keypedia.com/companies/manchester-va-medical-center/5c5a5d94-2ce9-4d93-bfb8-2936d91effb8

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