FDA Inspection
Hospi CorporationHospi Corporation – FDA Inspection, Mar 14, 2025
Record Details
This FDA Inspection record concerns Hospi Corporation, with an inspection on March 14, 2025, issued by the San Francisco District Office, covering medical devices & rad health.
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ID · 04deb5fb-0102-4912-8e58-10fa486a4935
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1263753
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Medical Devices
FDA Citations
2- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
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