# Henan Kangdi Medical Devices Co. Ltd – FDA Inspection, Dec 14, 2016

Source: https://www.keypedia.com/records/fda_inspections/henan-kangdi-medical-devices-co-ltd/a7859e8b-7b97-4747-b796-746ed6a82bc3
Source feed: FDA_Inspections

> FDA inspection 995883 of Henan Kangdi Medical Devices Co. Ltd, December 14, 2016. Classification: Voluntary Action Indicated (VAI). 13 citations under 21 CFR part 211. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 995883
- Company Name: Henan Kangdi Medical Devices Co. Ltd
- Inspection Date: 2016-12-14
- 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: 13

## Related Documents

- [FDA Inspection 1084134 - 2019-03-07](https://www.keypedia.com/records/fda_inspections/henan-kangdi-medical-devices-co-ltd/3ddf2003-ec69-4e13-b0a6-12ff64e9eacc)

## Related Officers

- [Satheesh Thomas](https://www.keypedia.com/people/satheesh-thomas/8009b8a5-40f5-4791-b0e9-a7c855e3afd4)

Company: https://www.keypedia.com/companies/henan-kangdi-medical-devices-co-ltd/27cc9024-4259-4761-bbf2-9c1bf3ddb827

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