# Dr. Sandeep Kumar Gupta – FDA Inspection, Aug 31, 2018

Source: https://www.keypedia.com/records/fda_inspections/dr-sandeep-kumar-gupta/e16d29df-c338-41de-84bf-5b08661c5877
Source feed: FDA_Inspections

> FDA inspection 1071165 of Dr. Sandeep Kumar Gupta, August 31, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1071165
- Company Name: Dr. Sandeep Kumar Gupta
- Inspection Date: 2018-08-31
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 0

## Related Documents

- FDA Inspection 766447 - 2012-01-18

## Related Officers

- [Company Rep](https://www.keypedia.com/people/kent-a-conforti/8d3d3e82-cd97-420e-8840-df92d6eeba09)

Company: https://www.keypedia.com/companies/dr-sandeep-kumar-gupta/b0883ef7-bbdf-4770-a610-2c4762b790f0

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