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483
•RLC Labs Inc.•November 2, 2023

RLC Labs Inc. – FDA 483, Nov 2, 2023

Record Details

RLC Labs Inc., an API Distributor and Dietary Supplement Manufacturer in Phoenix, AZ, was cited for a significant quality control deficiency. The firm failed to ensure the timely destruction of recalled drug products, despite a written commitment to the FDA made almost two years prior. This lapse indicates a failure of the quality control unit to fulfill its responsibilities and prevent the potential distribution of rejected drug products.

Company
RLC Labs Inc.
Inspection date
November 2, 2023
Product type
drugs
Office
Denver District Office
Person
  • Cecilia H. Kieu
View Company Profile

ID · 177c1f22-e20c-4bc1-8b53-7a77a3bf1193

Other documents for RLC Labs Inc.
  • 483 - 2023-09-15September 15, 2023
  • 483 - 2021-11-04November 4, 2021
  • WARNING_LETTER - 2020-03-05March 5, 2020
  • 483 - 2020-03-05March 5, 2020

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