# FDA 483 - Neocis, Inc. - December 11, 2019

Source: https://www.globalkeysolutions.net/records/483/neocis-inc/85490023-864c-40a8-8fa0-ffe899982e32

> FDA 483 for Neocis, Inc. on December 11, 2019. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Neocis, Inc.
- Inspection Date: 2019-12-11
- Product Type: device
- Office Name: Office of Medical Device and Radiological Health Division II
- Summary: Neocis, Inc., a medical device manufacturer in Miami, FL, was inspected by the FDA, resulting in one observation. The firm was cited for not adequately establishing requirements for its suppliers. This included deficiencies in supplier evaluation, control, and auditing procedures.

## Related Documents

- [483 - 2022-08-11](https://www.globalkeysolutions.net/records/483/neocis-inc/10976f80-d0b3-4e9c-a2db-4b95f49185b9)

## Related Officers

- [investigator](https://www.globalkeysolutions.net/people/stanley-b-eugene/4708f43e-0592-4c24-b276-d9f9092788a3)

Company: https://www.globalkeysolutions.net/companies/neocis-inc/e347cebf-7548-46b4-88ba-7a997fa684d3

Office: https://www.globalkeysolutions.net/offices/office-of-medical-device-and-radiological-health-division-ii/ae9bd439-479a-420d-9dd8-9fe1fc0863d6