Microbial contamination controls are not adequate.
Inspection Record
Lonza Houston, Inc — FDA 483 Findings
Inspectors Steven E BowenThe inspectors who signed the published document.Inspector lookup
View the regulator's official source The source document is always the basis for judgement.
Findings
The identity of each incoming batch of certain raw materials is not verified.
Written procedures are not always followed.
Physical and electronic control of material storage areas is not adequate.
About this record
Extracted automatically from the document US FDA published on 2021-01-14. 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.
