FDA Inspection
Leiluna, LLCLeiluna, LLC – FDA Inspection, Jan 17, 2025
Record Details
This FDA Inspection record concerns Leiluna, LLC, with an inspection on January 17, 2025, issued by the Florida District Office, covering foods & cosmetics.
View Company Profile
ID · ed05ce69-6276-4e11-89b3-407666fe0ea0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1232040
- FDA center
- Foods & Cosmetics
- Project area
- Colors and Cosmetics Technology
- Outcome
- Form 483 issued
FDA Citations
7- 21 CFR 111.560(a)Product complaint - qualified person review & investigate
- 21 CFR 111.70(e)Specifications - finished dietary supplement
- 21 CFR 111.205(a)Master manufacturing record - followed
- 21 CFR 111.510Returned dietary supplement - material review, disposition
- 21 CFR 111.260Batch record - required information
- 21 CFR 111.210Master manufacturing record - record requirements
- 21 CFR 111.120(e)Quality control operations - quarantine
Full citation text and observation details available on the Dashboard.
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.