1Process validation
Written production and process control procedures are not followed in the execution of production and process control functions.
Inspection Record
Kansas State Veterinary Diagnostic Laboratory — FDA 483 Findings
Inspectors Shafig AhadiThe inspectors who signed the published document.Inspector lookup
View the regulator's official source The source document is always the basis for judgement.
Findings
2Laboratory and QC controls
Laboratory records do not include a description of the sample received for testing, the lot number or other distinctive code of the sample and the date the sample was received for testing.
3Equipment and facility
Routine calibration of mechanical and electronic equipment is not performed according to a written program designed to assure proper performance.
4Documentation and records
Batch production and control records do not include complete information relating to the production and control of each batch.
About this record
Extracted automatically from the document US FDA published on 2026-10-19. 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.
