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483
•SOFIE Co. dba SOFIE•January 20, 2023

SOFIE Co. dba SOFIE – FDA 483, Jan 20, 2023

Record Details

An FDA inspection of SOFIE Co. dba SOFIE, a PET manufacturer in Somerset, NJ, revealed significant deficiencies across its quality system, production, laboratory controls, and facilities. Observations included widespread failure to follow written quality assurance procedures, inadequate investigations into deviations and out-of-specification results, and insufficient controls to ensure product quality and sterility. The firm also failed to properly handle complaints, validate test procedures, and maintain equipment suitability and cleanliness.

Company
SOFIE Co. dba SOFIE
Inspection date
January 20, 2023
Product type
drugs
Office
New Jersey District Office
People
  • Monika Borkowska (investigator)
  • Josh Renzo N. Ramilo
  • Doug Carre
  • Guerlain Ulysse (Investigator)
View Company Profile

ID · 8b5a4cdd-f4a2-4760-9a7b-eadf90984c84

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