# FDA 483 - Thornton Industries, Inc. - March 04, 2020

Source: https://www.keypedia.com/records/483/thornton-industries-inc/10fbf721-0c78-4f85-9f77-885de5e000ea

> FDA 483 for Thornton Industries, Inc. on March 04, 2020. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Thornton Industries, Inc.
- Inspection Date: 2020-03-04
- Product Type: drugs
- Office Name: Chicago District Office
- Summary: Thornton Industries, Inc. in Morris, IL, a drug manufacturer, was inspected by the FDA and received a Form 483 with four observations. The inspection revealed deficiencies in written procedures for sampling and testing, inadequate in-process controls and process validation, uncontrolled access to labeling materials, and a lack of identity testing for drug components. These issues indicate significant deviations from current Good Manufacturing Practices.

## Related Officers

- [Brian D. Nicholson](https://www.keypedia.com/people/brian-d-nicholson/83ea13dd-6753-468a-a0ca-19e3ef4158dd)

Company: https://www.keypedia.com/companies/thornton-industries-inc/93857b10-57cf-4666-9512-01da9b7cd7f2

Office: https://www.keypedia.com/offices/chicago-district-office/a510300b-0eaf-4a33-90b5-231d95977669