FDA Inspection 1135115 — Intertek USA Inc.
The FDA completed an inspection of Intertek USA Inc. on December 21, 2020 in Whitehouse, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- December 21, 2020
- Fiscal Year
- 2021
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Whitehouse, NJ (United States)