# Johnson Medtech LLC – FDA Inspection, Jun 6, 2019

Source: https://www.keypedia.com/records/fda_inspections/johnson-medtech-llc/07497275-0bc8-4369-8844-9fafe409cf95
Source feed: FDA_Inspections

> FDA inspection 1093160 of Johnson Medtech LLC, June 06, 2019. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1093160
- Company Name: Johnson Medtech LLC
- Inspection Date: 2019-06-06
- 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: 6

## Related Documents

- [FDA Inspection 1223759 - 2023-11-27](https://www.keypedia.com/records/fda_inspections/johnson-medtech-llc/7c8a6ca5-b18c-4b67-bc39-607a9d2d8fb2)
- FDA Inspection 1192743 - 2022-12-08

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/rosanna-m-goodrich/44c5c743-f67b-41fe-9cd1-8b5913bf580e)

Company: https://www.keypedia.com/companies/johnson-medtech-llc/b92b143a-21be-4a5d-ad5d-cced4ff6abc0

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