Home » C.R. Bard Form 483 Discusses Storage Area Control, DHR
C.R. Bard Form 483 Discusses Storage Area Control, DHR
C.R. Bard received an FDA Form 483 for storage area control and other manufacturing issues. The company had not performed temperature mapping studies to find “cold spots, hot spots, dead spots.”
The GMP Letter
Devices Inspections and Audits QualityThe GMP Letter
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