# Kerma Medical Products, Inc, Suffolk, VA – FDA Inspections

Source: https://www.keypedia.com/companies/kerma-medical-products-inc/bb96e435-46df-43ce-b968-771b7abe04f3

> Inspection records and compliance data for Kerma Medical Products, Inc in Suffolk, Virginia. 3 FDA inspections on record, last inspected July 07, 2017.

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## Details

- Name: Kerma Medical Products, Inc
- FEI Number: 1000123280
- Address Line 1: 215 Suburban Dr
- City: Suffolk
- State: Virginia
- Zip Code: 23434
- Country Name: United States
- Address: 215 Suburban Dr, Suffolk, Virginia 23434, United States
- Country: United States

## Related Documents

- FDA Inspection 1024609 - Kerma Medical Products, Inc - 2017-07-07 — classification: No Action Indicated (NAI), source: FDA, date: July 7, 2017
- FDA Inspection 1024609 - Kerma Medical Products, Inc - 2017-07-07 — classification: No Action Indicated (NAI), source: FDA, date: July 7, 2017
- [FDA Inspection 863395 - Kerma Medical Products, Inc - 2014-01-23](https://www.keypedia.com/records/fda_inspections/kerma-medical-products-inc/22972682-7e26-40de-ac5b-15f67e82e8d6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 23, 2014
- FDA Inspection 752181 - Kerma Medical Products, Inc - 2011-11-04 — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2011
- [FDA Inspection 752181 - Kerma Medical Products, Inc - 2011-11-04](https://www.keypedia.com/records/fda_inspections/kerma-medical-products-inc/7dd03706-42b3-4fee-aa7f-c76afab662a1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 4, 2011

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