# Synthexim – FDA Inspection, Feb 3, 2017

Source: https://www.keypedia.com/records/fda_inspections/synthexim/ec5a1ce0-0fb1-4abe-a704-5b6d8a6facf6
Source feed: FDA_Inspections

> FDA inspection 1002822 of Synthexim, February 03, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1002822
- Company Name: Synthexim
- Inspection Date: 2017-02-03
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 0

## Related Documents

- FDA Inspection 1228808 - 2022-09-08
- FDA Inspection 749514 - 2011-06-09

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/kham-phommachanh/cc7e728e-d2a1-469d-be3a-4f5fdd43b2dc)

Company: https://www.keypedia.com/companies/synthexim/1e3e16bc-7fae-4f53-bad1-784615f81b52

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