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483
•Omega Plastics Inc.•July 16, 2018

Omega Plastics Inc. – FDA 483, Jul 16, 2018

Record Details

Omega Plastics, Inc. in Clinton Township, MI, received a Form FDA 483 with six observations related to significant deficiencies in their quality system for medical device manufacturing. The inspection revealed issues with process validation, process controls, environmental controls in cleanrooms, corrective and preventive actions, quality audits, and control of nonconforming product. These findings indicate a need for comprehensive improvements across multiple critical manufacturing and quality assurance areas.

Company
Omega Plastics Inc.
Inspection date
July 16, 2018
Product type
device
Office
Division of Pharmaceutical Quality Operations III
People
  • Thomas A. Peter (Medical Device Senior Operations Officer at FDA)
  • Emilie E. Kahn (Regulatory Counsel, CDER Compliance, Office of Manufacturing Quality)
View Company Profile

ID · 55d048f9-93f6-4663-83ab-fd7a0777fb74

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