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483
•Phamatech•January 23, 2020

Phamatech – FDA 483, Jan 23, 2020

Record Details

Phamatech, a medical device manufacturer in San Diego, CA, was inspected by the FDA from January 17-23, 2020. The inspection revealed significant deficiencies in production process monitoring, complaint handling procedures, and the validation of critical manufacturing processes, specifically for HCG test devices. These issues indicate a lack of adequate quality system controls.

Company
Phamatech
Inspection date
January 23, 2020
Product type
device
Office
Division of Pharmaceutical Quality Operations IV
Person
  • Jenny L Mccardell
View Company Profile

ID · a91d8d3c-a325-4559-8de1-1d75ae35f1b6

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