FDA Inspection 1145198 — Qikmoov LLC

Qikmoov LLC — FEI 3017721316

The FDA completed an inspection of Qikmoov LLC on June 30, 2021 in Norwalk, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 30, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Norwalk, CA (United States)

Citations

IDCFRDescription
177721 CFR 211.150(b)Distribution Recall System
900121 CFR 211.22(a)Lack of quality control unit