# Junopacific Inc. – FDA Inspection, Jan 24, 2025

Source: https://www.keypedia.com/records/fda_inspections/junopacific-inc/fbb83f27-0250-4869-b22a-9df07b5486ea
Source feed: FDA_Inspections

> FDA inspection 1261810 of Junopacific Inc., January 24, 2025. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1261810
- Company Name: Junopacific Inc.
- Inspection Date: 2025-01-24
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Minneapolis District Office
- Citation Count: 2

## Related Documents

- FDA Inspection 1190592 - 2022-11-15
- FDA Inspection 987417 - 2016-07-20

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/christina-l-bigham/f3da8e26-4a8c-43a8-8070-349fe4500289)
- [Investigator](https://www.keypedia.com/people/shawn-choi/77845db3-46a3-4d0f-b94c-428bc251c0dc)

Company: https://www.keypedia.com/companies/junopacific-inc/9077fa59-f1f3-4c7f-80f1-c471f3320eca

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d