FDA Inspection 558804 — 3PL Worldwide Inc.
The FDA completed an inspection of 3PL Worldwide Inc. on January 22, 2009 in Southington, CT. 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
- January 22, 2009
- Fiscal Year
- 2009
- Product Type
- Drugs
- Project Area
- Unapproved and Misbranded Drugs
- Location
- Southington, CT (United States)