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