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•Aspen Biopharma Labs Pvt., Ltd.•September 21, 2024

FDA 483 - Aspen Biopharma Labs Pvt., Ltd. - September 21, 2024

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Record Details

Aspen Biopharma Labs Pvt Ltd in Rangareddy, Hyderabad, India, was cited for significant deficiencies across its API manufacturing operations. The inspection revealed severe data integrity issues, a non-functional Quality Unit, inadequate process validation, and poor facility and equipment maintenance, exacerbated by recent flood damage and ongoing renovations. These findings indicate a pervasive lack of control over critical manufacturing processes and documentation.

Company
Aspen Biopharma Labs Pvt., Ltd.
Inspection Date
September 21, 2024
Product Type
Drugs
Office
Office of Inspections and Investigations
People
  • Pushpa S. Jayasekara (Investigator)
  • Khalid M. Khan
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ID · 549a2e47-d3c8-431a-a7f8-70a44164ebcc

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