FDA Inspection 1221698 — RLC Labs Inc.

RLC Labs Inc. — FEI 3002523846

The FDA completed an inspection of RLC Labs Inc. on November 2, 2023 in Phoenix, AZ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 2, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Phoenix, AZ (United States)

Citations

IDCFRDescription
104921 CFR 211.22(a)Approve or reject components, products