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483
•Precipart Corp•February 25, 2021

Precipart Corp – FDA 483, Feb 25, 2021

Record Details

PRECIPART CORPORATION, a medical device manufacturer in Farmingdale, NY, was inspected by the FDA from February 23-25, 2021. The inspection resulted in one observation. The firm failed to maintain written Medical Device Reporting (MDR) procedures, specifically lacking an approval signature and effective date.

Company
Precipart Corp
Inspection date
February 25, 2021
Product type
device
Office
Division of Human and Animal Food Operations - East I
Person
  • Kwong P. Lee (investigator)
View Company Profile

ID · 4f0071a0-ad24-4a8a-8e8f-3f90806a849e

Other documents for Precipart Corp
  • 483 - 2018-02-09February 9, 2018

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