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483
•Darmerica, LLC•July 18, 2019

Darmerica, LLC – FDA 483, Jul 18, 2019

Record Details

Darmerica, LLC, an API repacker/relabeler in Casselberry, FL, was inspected by the FDA. The inspection revealed significant deficiencies in quality control, including a lack of OOS investigations for temperature excursions, inadequate supplier qualification and material release procedures, and unqualified/unvalidated equipment for API storage and transport. These issues indicate a severe lack of control over the quality and integrity of active pharmaceutical ingredients.

Company
Darmerica, LLC
Inspection date
July 18, 2019
Product type
drugs
Office
Office of Medical Device and Radiological Health Division II
Person
  • Saundrea A. Munroe (Drug Specialist / Drug Investigator)
View Company Profile

ID · bcdfeacd-3b2c-4109-b8f7-15aea715f1b0

Other documents for Darmerica, LLC
  • 483 - 2025-03-19March 19, 2025
  • WARNING_LETTER - 2025-03-19March 19, 2025
  • 483 - 2025-03-18March 18, 2025
  • EIR - 2022-03-11March 11, 2022
  • EIR - 2019-07-18July 18, 2019

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