# FDA Inspection 1231119 - ProMed Pharma, LLC - February 21, 2024

Source: https://www.keypedia.com/records/fda_inspections/promed-pharma-llc/af86cdec-25c4-4ecc-863d-49a6b3157a9b
Source feed: FDA_Inspections

> FDA inspection 1231119 of ProMed Pharma, LLC, February 21, 2024. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1231119
- Company Name: ProMed Pharma, LLC
- Inspection Date: 2024-02-21
- 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: 1

## Related Documents

- [FDA Inspection 1220556 - 2023-10-17](https://www.keypedia.com/records/fda_inspections/promed-pharma-llc/861655b5-384e-49ed-815e-7b4fc8618a90)
- FDA Inspection 1081391 - 2019-02-12
- [FDA Inspection 997496 - 2016-12-08](https://www.keypedia.com/records/fda_inspections/promed-pharma-llc/75081719-8014-42ce-a2df-3fa0ae1ebd16)
- FDA Inspection 899317 - 2014-10-06
- FDA Inspection 792003 - 2012-07-11

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/albert-l-nguyen/496338d0-71c4-43da-92f0-09515559d9fc)

Company: https://www.keypedia.com/companies/promed-pharma-llc/6c90c728-0e76-4c0a-8975-59ee146d3393

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