# FDA Inspection 1029319 - Saibal Kar, MD - October 20, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/saibal-kar-md/28f798d5-54aa-4b5c-82e0-36d32361223f
Source feed: FDA_Inspections

> FDA Inspection 1029319 for Saibal Kar, MD on October 20, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029319
- Company Name: Saibal Kar, MD
- Inspection Date: 2017-10-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1045010 - 2018-03-08](https://www.globalkeysolutions.net/records/fda_inspections/saibal-kar-md/2d891b2d-1acb-4ad2-806c-32a3555efdac)
- [FDA Inspection 844644 - 2013-07-20](https://www.globalkeysolutions.net/records/fda_inspections/saibal-kar-md/6280ccbc-91d7-478d-bf04-2aedbc92f19c)
- [FDA Inspection 818442 - 2013-02-14](https://www.globalkeysolutions.net/records/fda_inspections/saibal-kar-md/6f97f285-c124-4ef6-9014-c24b86bc1cc1)

Company: https://www.globalkeysolutions.net/companies/saibal-kar-md/88c240df-e4a4-4e75-893c-14ebb07ac889

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7