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Tag: FDA 483

FDA Inspection of Generic Manufacturing Facilities: What to Expect in 2026
  • Feb 1, 2026
  • Alyssa A
  • Pharmaceuticals
  • 3 Comments

FDA Inspection of Generic Manufacturing Facilities: What to Expect in 2026

Understand what happens during an FDA inspection of generic drug manufacturing facilities, from the six-system evaluation to FDA 483 responses and the new PreCheck program. Learn how to prepare and avoid common compliance failures.

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