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483
•Rockford Specialties•September 10, 2019

Rockford Specialties – FDA 483, Sep 10, 2019

Record Details

An FDA inspection of Rockford Specialties, a contract manufacturer in Loves Park, IL, revealed significant deficiencies in its quality management system. The firm failed to appoint a management representative for quality and did not ensure its quality policy was understood or implemented by employees, with one issue being a repeat observation from a previous inspection. These findings indicate a concerning lack of adherence to fundamental quality system requirements.

Company
Rockford Specialties
Inspection date
September 10, 2019
Product type
other
Office
Chicago District Office
Person
  • Jesse A. Vazquez (Medical Device Specialist)
View Company Profile

ID · 71bf1a08-f82a-4185-93b0-93ea198042c4

Other documents for Rockford Specialties
  • 483 - 2026-04-29April 29, 2026

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