# Highridge Medical LLC – FDA Inspection, Mar 1, 2018

Source: https://www.keypedia.com/records/fda_inspections/highridge-medical-llc/deed496c-00b6-439a-8796-2c7fb96354b5
Source feed: FDA_Inspections

> FDA inspection 1042767 of Highridge Medical LLC, March 01, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 803. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1042767
- Company Name: Highridge Medical LLC
- Inspection Date: 2018-03-01
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1043760 - 2018-01-17
- [FDA Inspection 898988 - 2014-10-06](https://www.keypedia.com/records/fda_inspections/highridge-medical-llc/cce0cae9-9147-468a-ae72-132eadd5040b)
- FDA Inspection 714332 - 2011-02-24

## Related Officers

- [Investigator](https://www.keypedia.com/people/kathleen-s-tormey/5e1abfe2-078a-4c61-bb98-3885f853a945)

Company: https://www.keypedia.com/companies/highridge-medical-llc/2942f26e-1c21-4a07-bb53-4ad4b846a382

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