FDA Inspection 895491 — Lumina Health Products, Inc.

Lumina Health Products, Inc. — FEI 3004395030

The FDA completed an inspection of Lumina Health Products, Inc. on September 8, 2014 in Sarasota, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 8, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Unapproved and Misbranded Drugs
Location
Sarasota, FL (United States)