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483
•Intas Pharmaceuticals Limited•February 17, 2017

Intas Pharmaceuticals Limited – FDA 483, Feb 17, 2017

Record Details

Intas Pharmaceuticals Limited, an API and drug product manufacturer in Ahmedabad, India, was cited for significant deficiencies during an FDA inspection. Observations included a lack of established written procedures for equipment cleaning and storage, as well as inadequate studies for pre-cleaning and hold times. Additionally, the firm failed to store Active Pharmaceutical Ingredients (API) under recommended temperature conditions, potentially compromising product quality.

Company
Intas Pharmaceuticals Limited
Inspection date
February 17, 2017
Product type
drugs
Office
Office of Inspections and Investigations
Person
  • Unnee Ranjan (Investigator)
View Company Profile

ID · 7b1a2fd4-c8a7-4787-b726-6d7bd5f27637

Other documents for Intas Pharmaceuticals Limited
  • WARNING_LETTER - 2025-09-17September 17, 2025
  • 483 - 2025-02-14February 14, 2025
  • 483 - 2024-01-24January 24, 2024
  • 483 - 2023-12-07December 7, 2023
  • 483 - 2023-05-12May 12, 2023

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