FDA Inspection 1299288 — LPNA Group Inc.

LPNA Group Inc. — FEI 1000120219

The FDA completed an inspection of LPNA Group Inc. on January 21, 2026 in Tonawanda, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 21, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Tonawanda, NY (United States)

Citations

IDCFRDescription
241921 CFR 211.198(a)Complaint Handling Procedure
360221 CFR 211.160(a)Deviations from laboratory control requirements
439121 CFR 211.180(e)(2)Items to cover on annual reviews