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483
•Pharmco Laboratories Inc.•September 22, 2021

Pharmco Laboratories Inc. – FDA 483, Sep 22, 2021

Record Details

Pharmco Laboratories Inc. in Titusville, FL, was inspected and received a Form 483 with 10 observations, indicating significant deficiencies in their drug manufacturing operations. The inspection revealed widespread issues including inadequate equipment cleaning and maintenance, poor facility upkeep, insufficient process and water system validations, and failures in quality control. Additionally, problems were identified with laboratory controls and the proper management of drug product reserve samples.

Company
Pharmco Laboratories Inc.
Inspection date
September 22, 2021
Product type
drugs
Office
Office of Medical Device and Radiological Health Division II
Person
  • Nicole E. Knowlton (Investigator )
View Company Profile

ID · 8047a27a-811d-40be-8578-1acbe1e7ba66

Other documents for Pharmco Laboratories Inc.
  • 483 - 2025-03-20March 20, 2025
  • WARNING_LETTER - 2015-11-30November 30, 2015

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