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# Cleaning Procedures Faulted at India’s Aurobindo
- URL: https://www.fdaweb.com/cleaning-procedures-faulted-at-indias-aurobindo/
- Published: 2017-01-26T12:00:00.000Z
- Updated: 2026-09-14T22:03:20.000Z
- Author: David McFarland
- Tags: Drugs, #legacy-id-D5137828

A 10/17-10/25/16 FDA inspection at Aurobindo Pharma, Borpatla Village, India, found that equipment cleaning procedures were not adequately validated. A just-released [FDA-483](http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/CDERFOIAElectronicReadingRoom/UCM535801.pdf?ref=fdaweb.com) shows the deviation from current good manufacturing practice regulations for active pharmaceutical ingredients.