FDA Inspection 1154306 — Hillyard GMP

Hillyard GMP — FEI 3009690111

The FDA completed an inspection of Hillyard GMP on October 8, 2021 in Saint Joseph, MO. 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
October 8, 2021
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Joseph, MO (United States)

Citations

IDCFRDescription
360321 CFR 211.160(b)Scientifically sound laboratory controls