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483
•Sivshree Medittex (India) Pvt. Ltd.•August 6, 2019

FDA 483 - Sivshree Medittex (India) Pvt. Ltd. - August 06, 2019

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Record Details

Sivshree Medittex (India) Pvt. Ltd., a contract manufacturer in Coimbatore, India, received a Form FDA 483 with three observations. The inspection revealed significant deficiencies including the absence of written Medical Device Reporting procedures, a lack of written agreements with suppliers for change notification, and inadequate procedures for equipment calibration. These findings highlight critical gaps in the firm's quality system.

Company
Sivshree Medittex (India) Pvt. Ltd.
Inspection Date
August 6, 2019
Product Type
Device
Office
Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)
Person
  • Paul M. Kawamoto (issuing_officer)
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ID · 8fd2f49e-e887-4f86-816a-78c595e863eb

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