# Imediplus Inc. – FDA Inspection, Feb 22, 2019

Source: https://www.keypedia.com/records/fda_inspections/imediplus-inc/ac0f4e65-5118-4db0-8e01-f3032807242d
Source feed: FDA_Inspections

> FDA inspection 1082530 of Imediplus Inc., February 22, 2019. 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1082530
- Company Name: Imediplus Inc.
- Inspection Date: 2019-02-22
- Project Area: Compliance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 2

## Related Officers

- [Company Rep](https://www.keypedia.com/people/kwong-p-lee/f4778925-1fad-4988-9e39-86482896c4fa)

Company: https://www.keypedia.com/companies/imediplus-inc/b67ae7fe-e878-4a98-983b-ef03d58abe6a

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8