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483
•STERITECH, INC.•February 10, 2021

STERITECH, INC. – FDA 483, Feb 10, 2021

Record Details

STERITECH, INC., a contract sterilization facility in Salinas, PR, was inspected by the FDA from February 3-10, 2021. The inspection revealed significant deficiencies in the firm's corrective and preventive action (CAPA) system, including a lack of established procedures and inadequate documentation of CAPA activities and effectiveness checks. Additionally, production processes were not consistently monitored to ensure devices conformed to specifications, with temperature deviations noted during batch record reviews.

Company
STERITECH, INC.
Inspection date
February 10, 2021
Product type
device
Office
Office of Medical Device and Radiological Health Division II
Person
  • Maricelys Mercado (investigator)
View Company Profile

ID · ac6cf11e-bc92-471e-a3a5-ee3b76bf4d35

Other documents for STERITECH, INC.
  • 483 - 2023-12-08December 8, 2023
  • EIR - 2021-02-10February 10, 2021
  • EIR - 2019-02-19February 19, 2019

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