Aseptic processing areas are deficient regarding the system for monitoring environmental conditions.
Inspection Record
Talon Compounding Pharmacy — FDA 483 Findings
View the regulator's official source The source document is always the basis for judgement.
Findings
There is a failure to thoroughly review the failure of a batch or any of its components to meet any of its specifications whether or not the batch has been already distributed.
Clothing of personnel engaged in the processing of drug products is not appropriate for the duties they perfo rmed .
Time limits are not established when appropriate for the completion of each production phase to assure the quality of the drug product.
Aseptic processing areas are deficient regarding the system for cleaning and disinfecting the equipment to produce aseptic conditions.
Procedures designed to prevent microbiological contamination of drug products purporting to be sterile are not established, written and followed.
Aseptic processing areas are deficient regarding systems for maintaining any equipment used to control the aseptic conditions.
Each batch of drug product purporting to be sterile and pyrogen-free is not laboratory tested to determine conformance to such requirements.
Procedures designed to prevent microbiological contamination of drug products purporting to be sterile do not include adequate validation of the sterilization process.
The written stability testing program is not followed.
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.
