# Norfolk Medical Products, Inc. – FDA Inspection, Nov 2, 2018

Source: https://www.keypedia.com/records/fda_inspections/norfolk-medical-products-inc/f70938c8-f091-4016-ba24-5eec3f51d1e8
Source feed: FDA_Inspections

> FDA inspection 1071013 of Norfolk Medical Products, Inc., November 02, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1071013
- Company Name: Norfolk Medical Products, Inc.
- Inspection Date: 2018-11-02
- 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: 1

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## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jesse-a-vazquez/cac5b170-d0ea-4355-af5d-3d81546ff0fe)

Company: https://www.keypedia.com/companies/norfolk-medical-products-inc/a2db596b-8351-4825-84cf-ed707065318d

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