483
UIH Technologies LLCFDA 483 - UIH Technologies LLC - August 20, 2025
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An FDA inspection of UIH Technologies LLC, a medical device contract manufacturer in Houston, TX, revealed three significant observations. These included deficiencies in medical device labeling regarding Unique Device Identifiers (UDI), inadequate procedures for receiving and evaluating complaints, and insufficient establishment of finished device acceptance procedures. These findings indicate issues within the firm's quality system.
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