FDA Inspection 828887 — Air Liquide Electronics US LP
The FDA completed an inspection of Air Liquide Electronics US LP on April 17, 2013 in Morrisville, PA. 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
- April 17, 2013
- Fiscal Year
- 2013
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Morrisville, PA (United States)