Failure to fulfil the responsibilities of the Quality Control Unit.
Inspection Record
Biocon Ltd. — FDA 483 Findings
View the regulator's official source The source document is always the basis for judgement.
Findings
Equipment used in production operations are not adequately qualified.
Failure to adequately handle, store and document material movement and status.
Failure to perfonn adequately investigate non-confonnances.
About this record
Extracted automatically from the document US FDA published on 2020-03-06. The source is available at the link above.
This is a record of that moment. Inspection findings are usually followed by the company's response and corrective action, but this page does not know how that turned out. Do not read it as the current state; check the regulator's official announcements for the latest status.
Translation and classification are automated and may differ in nuance from the source.
