Inspection Record

Talon Compounding Pharmacy — FDA 483 Findings

US FDAInspected 2016-05-19Published 2024-01-17 10 findingsTraining and personnelAseptic processing and sterility assuranceStability and storageDeviation, CAPA, and investigationMaterial and supplier control

View the regulator's official source The source document is always the basis for judgement.

Findings

1Training and personnel

Clothing of personnel engaged in the processing of drug products is not appropriate for the duties they perform.

2Aseptic processing and sterility assurance

Aseptic processing areas are deficient regarding the system for cleaning and disinfecting the room to produce aseptic conditions.

3Aseptic processing and sterility assurance

Aseptic processing areas are deficient regarding the system for monitoring environmental conditions.

4Aseptic processing and sterility assurance

Aseptic processing areas are deficient regarding systems for maintaining any equipment used to control the aseptic conditions.

5Aseptic processing and sterility assurance

Each batch of drug product purporting to be sterile is not laboratory tested to determine conformance to such requirements.

6Stability and storage

There is no written testing program designed to assess the stability characteristics of drug products.

7Deviation, CAPA, and investigation

Investigations of a failure of a batch or any of its components to meet any of its specifications did not extend to other drug products that may have been associated with the specific failure or discrepancy.

8Aseptic processing and sterility assurance

Procedures designed to prevent microbiological contamination of drug products purporting to be sterile do not include validation of the sterilization process.

9Material and supplier control

There was a failure to handle and store components at all times in a manner to prevent contamination.

10Aseptic processing and sterility assurance

Procedures designed to prevent microbiological contamination of drug products purporting to be sterile are 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.

Other records for this company

Talon Compounding Pharmacy company profile — full history US FDA documents, 2024 Go to Findings search