FDA Inspection 1078690 — Precision Dose Inc.

Precision Dose Inc. — FEI 1419861

The FDA completed an inspection of Precision Dose Inc. on Jan 28, 2019 in South Beloit, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 28, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
South Beloit, IL (United States)

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