483
RLC Labs Inc.FDA 483 - RLC Labs Inc. - November 04, 2021
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RLC Labs Inc., a manufacturer in Phoenix, AZ, was cited for two observations during an FDA inspection. The firm failed to ensure complete backup data for temperature/humidity monitoring in its materials warehouse and lacked a routine calibration program for the monitoring equipment used to store finished drug thyroid tablets and active pharmaceutical ingredients. These issues indicate deficiencies in data integrity and equipment control.
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