FDA Inspection
Intertek USA, Inc.Intertek USA, Inc. – FDA Inspection, Nov 9, 2017
Record Details
This FDA Inspection record concerns Intertek USA, Inc., with an inspection on November 9, 2017, issued by the Los Angeles District Office, covering human drugs.
- People
- Lakecha N. Lewis (FDA Associated Person)
- Mohsen Rajabi Abhari (Issuing Officer)
View Company Profile
ID · c2ecde5f-09be-4e03-9e5b-8646df813f80
Inspection Facts
- Inspection number
- 1031185
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
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