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483
•Atalys Asheboro LLC•July 23, 2021

Atalys Asheboro LLC – FDA 483, Jul 23, 2021

Record Details

An FDA inspection of FPE NC LLC, a medical device manufacturer in Asheboro, NC, revealed significant deficiencies in their quality system. The firm failed to establish written procedures for Medical Device Reporting (MDR), adequately manage complaints, and properly document corrective and preventive actions. These issues indicate a lack of robust quality control processes.

Company
Atalys Asheboro LLC
Inspection date
July 23, 2021
Product type
device
Office
Atlanta District Office
Person
  • Christopher B. May
View Company Profile

ID · 21830015-0047-483b-99ad-d577a5bd9848

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