Findings
1Quality unit oversight
Your firm failed to establish an adequate quality control unit with the responsibility and authority to approve or reject all components, drug product containers, closures, in-process materials, packaging materials, labeling, and drug products (21 CFR 211.22(a)). The records and information you provided demonstrate that your quality unit (QU) did not effectively exercise its responsibilities to oversee the quality of your drug manufacturing operations. Your QU is responsible…
2Documentation and records
Your firm failed to have, for each batch of drug product, appropriate laboratory determination of satisfactory conformance to final specifications for the drug product, including the identity and strength of each active ingredient, prior to release (21 CFR 211.165(a)). Based on the records and information you provided, you did not demonstrate that you conducted adequate finished drug product testing on your drug products. For example, the SOPURE ANTISEPTIC SKIN CLEANSER hand sanitizer batch records that you provided, do not include an appropriate assay test for active ingredient content or adequate impurity testing. Your firm conducts alcohol content testing by measuring density using hydrometer equipment, and tests for methanol and (b)(4) through organoleptic inspection for odor. Full release testing, including strength and identity testing of the active ingredient, must be performed before drug product release and distribution. Without adequate testing, you do not have adequate scientific evidence to assure that your drug products conform to appropriate specifications before release.
3Stability and storage
Your firm failed to establish and follow an adequate written testing program designed to assess the stability characteristics of drug products and to use results of stability testing to determine appropriate storage conditions and expiration dates (21 CFR 211.166(a)). Based on the records and information you provided, you failed to provide adequate stability data to demonstrate that the chemical properties of your SOPURE ANTISEPTIC SKIN CLEANSER hand sanitizers remain…
About this record
Extracted automatically from the document US FDA published on 2024-09-17. 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.
