1Laboratory and QC controls
Each batch of drug product required to be free of objectionable microorganisms is not tested through appropriate la boratory testing.
Inspection Record
Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical — FDA 483 Findings
View the regulator's official source The source document is always the basis for judgement.
Findings
2Labeling and packaging
The labels of your outsourcing facility’s drug products are deficient.
3Aseptic processing and sterility assurance
Aseptic processing area deficient regarding the system for monitoring environmental conditions.
4Aseptic processing and sterility assurance
Drug product containers and closures were not sterilized and processed to remove pyrogenic properties to assure that they are suitable for their intended useDrug product containers and closures were not sterilized and processed to remov e pyrogenic properties to assure that they are suitable for their intended use Specifically, A.
5Aseptic processing and sterility assurance
Procedures designed to prevent microbiological contamination of drug products purporting to be sterile are not establishe d.
6Regulatory reporting and change control
Your outsourcing facility did not submit an initial report to fda identifying products compounded during the previous si x months as required by section 503B(b)(2)(A).
About this record
Extracted automatically from the document US FDA published on 2025-06-20. 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.
