FDA Inspection 1281826 — Precision Dose Inc.

Precision Dose Inc. — FEI 1419861

The FDA completed an inspection of Precision Dose Inc. on September 11, 2025 in South Beloit, IL. 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
September 11, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
South Beloit, IL (United States)

Citations

IDCFRDescription
110521 CFR 211.22(d)Procedures not in writing, fully followed
358221 CFR 211.105(a)Identification of containers, lines, equipment