# FDA 483 - Azico Biophore India Private Limited - September 01, 2025

Source: https://www.keypedia.com/records/483/azico-biophore-india-private-limited/e4424993-a9f7-47d7-8c8d-3360f7a67b79

> FDA 483 for Azico Biophore India Private Limited on September 01, 2025. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Azico Biophore India Private Limited
- Inspection Date: 2025-09-01
- Product Type: drugs
- Office Name: Office of Partnerships
- Summary: An FDA inspection of Azico Biophore India Private Limited, an API manufacturer, revealed significant deficiencies in their cleaning validation processes. The firm failed to adequately evaluate endotoxin contamination for equipment used in manufacturing sterile APIs and did not conduct comprehensive impact assessments for changes to critical cleaning validation procedures. These issues indicate a lack of robust quality control for products intended for sterile finished dosage drug products.

## Related Documents

- [483 - Unknown Date](https://www.keypedia.com/records/483/azico-biophore-india-private-limited/1f5a67a2-d2b4-4319-94fb-e12c76e27adb)

## Related Officers

- [Consumer Safety Officer, FDA](https://www.keypedia.com/people/conner-n-mann/626fec03-b389-435c-b038-376fcc0952ac)

Company: https://www.keypedia.com/companies/azico-biophore-india-private-limited/373fe2a1-5910-425f-8478-71be63a40f32

Office: https://www.keypedia.com/offices/office-of-partnerships/83acc701-fc5a-4876-bb34-7499e31541d3