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483
•Plantex Ltd.

Plantex Ltd. – FDA 483

Record Details

An FDA inspection of Plantex Ltd. in Netanya, Israel, revealed significant data integrity and quality control deficiencies. Observations included unauthorized data access and deletion, inadequate test procedures for raw materials and APIs, and insufficient equipment cleaning protocols for microbiological and endotoxin contamination. These issues indicate a lack of robust controls over manufacturing processes and data management.

Company
Plantex Ltd.
Product type
drugs
Office
Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
People
  • Leonard H. Lavi (Investigative Engineer )
  • Sandra A. Hughes
View Company Profile

ID · 0448e4ec-e16f-4a88-b5c6-69790dd9dd64

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