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483
•Syenz Laboratory, LLC•March 5, 2020

Syenz Laboratory, LLC – FDA 483, Mar 5, 2020

Record Details

Syenz Laboratory, LLC, an Own Label Distributor and Control Testing Laboratory in Norwood, NJ, received a Form 483 with eight observations related to significant deficiencies in its quality control, distribution, complaint handling, and laboratory control systems. The firm failed to adequately review batch records, maintain distribution documentation, establish complaint procedures, test components, ensure representative sampling, implement stability testing, conduct microbial testing, and retain reserve samples for its OTC drug products. These issues indicate a lack of robust quality oversight and control over its drug product manufacturing and distribution processes.

Company
Syenz Laboratory, LLC
Inspection date
March 5, 2020
Product type
drugs
Office
New Jersey District Office
Person
  • Helen Verdel (Director of Clinical Training)
View Company Profile

ID · 79aaf539-0b90-4a12-bbe0-0ee3680dc8ea

Other documents for Syenz Laboratory, LLC
  • 483 - 2022-09-30September 30, 2022

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