# FDA 483 - Med Systems - March 14, 2025

Source: https://www.keypedia.com/records/483/med-systems/6bb51bd6-3237-46b6-bab7-70466c3bfb3a

> FDA 483 for Med Systems on March 14, 2025. Product: device. Access full analysis and detailed observations.

---

## Details

- Record Type: 483
- Company Name: Med Systems
- Inspection Date: 2025-03-14
- Product Type: device
- Office Name: Los Angeles District Office
- Summary: Med Systems INC., a manufacturer of the Class 2 medical device Electro Flo 5000, was inspected by the FDA. The inspection revealed one observation concerning the firm's failure to adequately establish and maintain records for the evaluation and reevaluation of its suppliers. This indicates a deficiency in their quality system regarding supplier management.

## Related Officers

- [Juanj Wu](https://www.keypedia.com/people/juanj-wu/0d3e8970-b524-49f6-a307-079091b3c91d)

Company: https://www.keypedia.com/companies/med-systems/9e357c5e-0b4d-455d-8355-7a756e4dff02

Office: https://www.keypedia.com/offices/los-angeles-district-office/edcf1dfe-596a-43b8-8df4-07d9cd94763b