FDA Inspection 1151828 — Philips Image Guided Therapy Corporation

Philips Image Guided Therapy Corporation — FEI 3016257349

The FDA completed an inspection of Philips Image Guided Therapy Corporation on August 27, 2021 in Plymouth, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 27, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Plymouth, MN (United States)