# FDA 483 - Helio USA Inc - September 26, 2011

Source: https://www.globalkeysolutions.net/records/483/helio-usa-inc/9f3fb356-a014-4674-b12a-371bbf02e64a

> FDA 483 for Helio USA Inc on September 26, 2011. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Helio USA Inc
- Inspection Date: 2011-09-26
- Product Type: device
- Office Name: Division of Human and Animal Food Operations - West V
- Summary: Helio Medical Supplies Inc. in San Jose, CA, was inspected and cited for significant deficiencies across its quality system. The inspection revealed a lack of established procedures for design control, complaint handling, corrective and preventive actions, and purchasing controls. Additionally, issues with supplier agreements, incoming product acceptance, document control, and personnel training were identified, indicating a systemic breakdown in quality management for their medical devices, including acupuncture needles and infrared heat lamps.

## Related Officers

- [investigator](https://www.globalkeysolutions.net/people/mark-e-chan/2a5a3abf-96f6-4ceb-b87d-379ed5c6f47e)

Company: https://www.globalkeysolutions.net/companies/helio-usa-inc/5c2e6761-b856-452e-8b37-2ecc0aa37dc4

Office: https://www.globalkeysolutions.net/offices/division-of-human-and-animal-food-operations-west-v/0f4dd01e-8e8a-4336-9abe-ce8b3d309e8b