FDA Inspection
Lucideon LimitedLucideon Limited – FDA Inspection, Sep 10, 2019
Record Details
This FDA Inspection record concerns Lucideon Limited, with an inspection on September 10, 2019, issued by the Office of Inspections and Investigations, covering human drugs.
View Company Profile
ID · 3937f69e-b160-4cee-8dc4-cbbc5a06cccc
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1101554
- FDA center
- Human Drugs
- Project area
- New Drug Evaluation
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 211.160(b)Scientifically sound laboratory controls
- 21 CFR 211.192Written record of investigation incomplete
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Lucideon Limited
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 29, 2024 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Lucideon Limited
- FDA Inspection 1245602 - 2024-02-29
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.