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483
•Seven•April 8, 2021

Seven – FDA 483, Apr 8, 2021

Record Details

Seven, a contract manufacturer of dietary supplements in Vista, CA, was cited for numerous significant quality control and documentation deficiencies during an FDA inspection. The firm failed to establish and adhere to specifications for components, finished products, and packaging, and lacked proper quality control oversight for material review, batch records, and master manufacturing records. Several observations were noted as repeat violations, indicating persistent issues with their manufacturing processes.

Company
Seven
Inspection date
April 8, 2021
Product type
other
Office
Division of Pharmaceutical Quality Operations IV
People
  • Elizabeth C. Ajuzie
  • Natalie J. Reese
View Company Profile

ID · 4c1d9c40-585c-452e-beab-ed8b124b278c

Other documents for Seven
  • WARNING_LETTER - 2019-08-19August 19, 2019

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