Procedures designed to assure that correct labeling and packaging materials are used for chug products are not written and followed.
Inspection Record
Sincerus Florida, LLC. — FDA 483 Findings
View the regulator's official source The source document is always the basis for judgement.
Findings
Procedures designed to prevent microbiological contamination of drng products pmp orting to be sterile are not followed.
The labels of your outsourcing facility's drug products are deficient.
About this record
Extracted automatically from the document US FDA published on 2024-01-17. 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.
