FDA Inspection
ProMed Pharma, LLCFDA Inspection 1231119 - ProMed Pharma, LLC - February 21, 2024
Record Details
This FDA Inspection record concerns ProMed Pharma, LLC, with an inspection on February 21, 2024, issued by the Center for Devices and Radiological Health, covering devices.
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ID · af86cdec-25c4-4ecc-863d-49a6b3157a9b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1231119
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of ProMed Pharma, LLC
5| Date | Classification | Office | Project area |
|---|---|---|---|
| October 17, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 12, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 8, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 6, 2014 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| July 11, 2012 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for ProMed Pharma, LLC
- FDA Inspection 1220556 - 2023-10-17
- FDA Inspection 1081391 - 2019-02-12
- FDA Inspection 997496 - 2016-12-08
- FDA Inspection 899317 - 2014-10-06
- FDA Inspection 792003 - 2012-07-11
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