# FDA Inspection 981650 - Intertek USA Inc. - August 12, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/intertek-usa-inc/55df2482-54f0-4339-9b35-8ddf9cc459fb/
Source feed: FDA_Inspections

> FDA Inspection 981650 for Intertek USA Inc. on August 12, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 981650
- Company Name: Intertek USA Inc.
- Inspection Date: 2016-08-12
- Classification: No Action Indicated (NAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

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Company: https://www.globalkeysolutions.net/companies/intertek-usa-inc/2c61102d-28cb-4e8b-b5c0-01d3148f07d0

Office: https://www.globalkeysolutions.net/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c