FDA Inspection 981650 — Intertek USA Inc.
The FDA completed an inspection of Intertek USA Inc. on Aug 12, 2016 in Whitehouse, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Aug 12, 2016
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Whitehouse, NJ (United States)