# Intertek USA, Inc. – FDA Inspection, Nov 9, 2017

Source: https://www.keypedia.com/records/fda_inspections/intertek-usa-inc/c2ecde5f-09be-4e03-9e5b-8646df813f80
Source feed: FDA_Inspections

> FDA inspection 1031185 of Intertek USA, Inc., November 09, 2017. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031185
- Company Name: Intertek USA, Inc.
- Inspection Date: 2017-11-09
- Product Type: Human Drugs
- Center: Human Drugs
- Office Name: Los Angeles District Office
- Citation Count: 0

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/lakecha-n-lewis/39b6305d-2a9f-448b-9a14-e412b43c8522)
- Issuing Officer

Company: https://www.keypedia.com/companies/intertek-usa-inc/23ab26e6-fc8f-48b9-ac05-cba280eebd24

Office: https://www.keypedia.com/offices/los-angeles-district-office/edcf1dfe-596a-43b8-8df4-07d9cd94763b