# FDA 483 - Rhodes Technologies - July 27, 2016

Source: https://www.keypedia.com/records/483/rhodes-technologies/52f63025-0aa7-44ff-af28-cb1cdf793e3c

> FDA 483 for Rhodes Technologies on July 27, 2016. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Rhodes Technologies
- Inspection Date: 2016-07-27
- Product Type: drugs
- Office Name: Division of Northeast Imports 
- Summary: An FDA inspection of Rhodes Technologies in Coventry, RI, revealed significant deficiencies in the firm's Quality Unit operations. Observations included failures to identify unknown peaks during residual solvent analysis, inadequate investigation of out-of-specification microbial content results, and multiple failures to adequately investigate deviations related to their stability program. These issues highlight systemic problems in quality control and investigation processes.

## Related Officers

- [Investigator](https://www.keypedia.com/people/erik-w-koester/2bbab081-6783-40a1-83c1-b219bde22bd1)

Company: https://www.keypedia.com/companies/rhodes-technologies/d7ffefee-10ee-4ec3-aee8-29ded242ee2d

Office: https://www.keypedia.com/offices/division-of-northeast-imports/b20599cf-9797-41fd-947f-6589ef596a94