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483
•Inga Pharmaceuticals•June 12, 2017

Inga Pharmaceuticals – FDA 483, Jun 12, 2017

Record Details

Inga Pharmaceutical, a manufacturer in Tambaram, Chennai, India, was cited for significant deficiencies during an FDA inspection. Observations included inadequate instrument calibration, lack of label control procedures, and widespread failures within the quality unit regarding procedure adherence, scientific justification, and instruction specificity. The firm also lacked a defined sanitization frequency and failed to validate an Excel worksheet used for critical calculations.

Company
Inga Pharmaceuticals
Inspection date
June 12, 2017
Product type
drugs
Office
Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
Person
  • Ariel Cruz Figueroa (Retired)
View Company Profile

ID · 8edaf72b-a2fb-4f60-b740-e8255572b063

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