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Home > Newsletters > The GMP Letter > Electro-Cap Handed 483 for Validation Procedure Lapses

The GMP Letter

July 2012

Electro-Cap Handed 483 for Validation Procedure Lapses

The FDA’s Cincinnati District Office issued a Form 483 to a maker of electroencephalogram application caps and related supplies due to missing validation and control procedures at its Eaton, Ohio, plant.

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