FDA Inspection
USpharma, Ltd., Co.USpharma, Ltd., Co. – FDA Inspection, May 11, 2023
Record Details
This FDA Inspection record concerns USpharma, Ltd., Co., with an inspection on May 11, 2023, issued by the Center for Devices and Radiological Health, covering devices.
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ID · aebff30a-bd8c-4932-a30d-d8f250541cb5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1205546
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
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Other FDA inspections of USpharma, Ltd., Co.
7| Date | Classification | Office | Project area |
|---|---|---|---|
| September 3, 2026 | VAI | Florida District Office | Drug Quality Assurance |
| September 1, 2026 | Not classified | Florida District Office | |
| February 16, 2023 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 23, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 3, 2015 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for USpharma, Ltd., Co.
- FDA Inspection 1334262 - 2026-09-03
- FDA Inspection 1334958 - 2026-09-01
- FDA Inspection 1198249 - 2023-02-16
- FDA Inspection 1172561 - 2022-06-23
- FDA Inspection 912614 - 2015-02-03
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