# iCRco, Inc. – FDA 483, Jul 17, 2026

Source: https://www.keypedia.com/records/483/icrco-inc/9235563e-25dc-47b5-9158-7d926c5613b3

> FDA 483 for iCRco, Inc. on July 17, 2026. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: iCRco, Inc.
- Inspection Date: 2026-07-17
- Product Type: device
- Office Name: Los Angeles District Office
- Summary: iCRco, Inc. in Goleta, CA, a medical device manufacturer, received a Form FDA 483 with two observations. The inspection revealed deficiencies in the firm's quality system, specifically regarding the inadequate maintenance of records for process validation and supplier monitoring. These issues indicate a need for improved documentation practices to ensure compliance.

## Related Documents

- [483 - 2022-07-01](https://www.keypedia.com/records/483/icrco-inc/86f0a3ad-4065-425e-8a9c-62931bb0ce68) — date: July 1, 2022

## Related Officers

- [investigator](https://www.keypedia.com/people/sarah-a-hassas/4f142d54-fc28-4bd5-82ad-7e6fa443688c)

Company: https://www.keypedia.com/companies/icrco-inc/9cbe0ad8-2b62-4275-8711-3879dbf1064d

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