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483
•InvaTech Pharma Solutions, LLC•February 5, 2019

InvaTech Pharma Solutions, LLC – FDA 483, Feb 5, 2019

Record Details

InvaTech Pharma Solutions LLC, a drug manufacturer in East Brunswick, NJ, received a Form 483 with two observations during an FDA inspection. The firm failed to thoroughly investigate an unexplained discrepancy related to a batch of tablets and did not conduct documented annual cGMP training for its employees. These findings indicate deficiencies in the firm's quality system and personnel training.

Company
InvaTech Pharma Solutions, LLC
Inspection date
February 5, 2019
Product type
drugs
Office
New Jersey District Office
Person
  • Yvesna Blaise
View Company Profile

ID · 2690f600-078e-48b8-9c11-01e002f1066a

Other documents for InvaTech Pharma Solutions, LLC
  • 483 - 2026-05-13May 13, 2026
  • 483 - 2023-06-09June 9, 2023
  • 483 - 2017-12-28December 28, 2017
  • 483 - 2017-04-04April 4, 2017

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