# FDA 483 - A.I.G Technologies Inc. - July 01, 2011

Source: https://www.keypedia.com/records/483/aig-technologies-inc/53d9976c-d453-4b5c-b129-699226c1fdcb

> FDA 483 for A.I.G Technologies Inc. on July 01, 2011. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: A.I.G Technologies Inc.
- Inspection Date: 2011-07-01
- Product Type: drugs
- Office Name: Office of Medical Device and Radiological Health Division II
- Summary: A.I.G Technologies, Inc. in Deerfield Beach, FL, was cited with nine observations during an FDA inspection from June 27 to July 1, 2011, highlighting significant deficiencies across its manufacturing operations. The firm lacked a functional quality control unit, proper employee training, and adequate sanitation practices. Key issues included failures in record-keeping for equipment and processes, insufficient material control, and a lack of validated procedures for production and product preservation, indicating a broad non-compliance with good manufacturing practices.

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## Related Officers

- [Kimberly M. Hull](https://www.keypedia.com/people/kimberly-m-hull/dd9a4388-b2e8-4782-ae47-1b4cb5de35c0)

Company: https://www.keypedia.com/companies/aig-technologies-inc/93f0cba6-de77-4b63-8121-61987aab0949

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