# Kem Medical Products Corp – FDA Inspection, Jul 21, 2022

Source: https://www.keypedia.com/records/fda_inspections/kem-medical-products-corp/50793f7c-11b8-4d87-a61a-7778ec2b683c
Source feed: FDA_Inspections

> FDA inspection 1175436 of Kem Medical Products Corp, July 21, 2022. Classification: Voluntary Action Indicated (VAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1175436
- Company Name: Kem Medical Products Corp
- Inspection Date: 2022-07-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1115221 - 2020-01-15](https://www.keypedia.com/records/fda_inspections/kem-medical-products-corp/a27e28e9-6290-4f2c-b798-6b3e218a03ed)
- FDA Inspection 1003651 - 2017-02-21
- FDA Inspection 791042 - 2012-07-10
- [FDA Inspection 623870 - 2009-10-27](https://www.keypedia.com/records/fda_inspections/kem-medical-products-corp/19622308-fea7-4b95-bf14-6ef3e8e52cc1)

Company: https://www.keypedia.com/companies/kem-medical-products-corp/839eba3c-ce65-4e39-a7a5-7258eddea42a

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