# AMPCARE, LLC – FDA Inspection, Nov 15, 2017

Source: https://www.keypedia.com/records/fda_inspections/ampcare-llc/a15cc2be-85ed-4c30-9637-26bb15e314b5
Source feed: FDA_Inspections

> FDA inspection 1031825 of AMPCARE, LLC, November 15, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031825
- Company Name: AMPCARE, LLC
- Inspection Date: 2017-11-15
- 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 1287414 - 2025-09-25](https://www.keypedia.com/records/fda_inspections/ampcare-llc/5611cf07-7033-40a1-b82d-2978c91b32f0)
- FDA Inspection 1204300 - 2023-04-26
- FDA Inspection 902431 - 2014-11-04

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/iris-c-macinnes/5e8d7fef-18d5-453d-82b2-19e8e2897d26)

Company: https://www.keypedia.com/companies/ampcare-llc/3d1334e9-63ab-4784-ac93-c5b3bc1c789b

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