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Home » Photonic Gets 483 for Repeat Deficient Design, CAPA and MDR Procedures
Photonic Gets 483 for Repeat Deficient Design, CAPA and MDR Procedures
The FDA issued Photonic Health an eight-observation Form 483 after an inspection of the company’s Ocala, Fla., facility in March found the firm had failed to address deficiencies observed in a previous inspection.