Testing and release of drug product for distribution do not include appropriate laboratory determinatio n of satisfactory conformance to the identity and strength of each active ingredient prior to release.
Inspection Record
Bedford Pharmacy Inc. — FDA 483 Findings
Inspectors Stacey S Degarmo · John P MistlerThe inspectors who signed the published document.Inspector lookup
View the regulator's official source The source document is always the basis for judgement.
Findings
Aseptic processing areas are deficient regarding the system for cleaning and disinfecting the equipment to produce aseptic conditions.
Aseptic processing areas are deficient regarding systems for maintaining any equipment used to control the aseptic conditions.
Drug products do not bear an expiration date determined by appropriate stability data to assure they meet applicable standards of identity, strength, quality and purity at the time of use.
Each batch of drug product required to be free ofobjectionable microorganisms is not tested throug h appropriate laboratory testing.
Aseptic processing areas are deficient regarding the system for monitoring environmental conditions.
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.
