FDA Inspection 1253785 — Portable Therapeutix

Portable Therapeutix — FEI 3010201075

The FDA completed an inspection of Portable Therapeutix on Nov 12, 2024 in Houston, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 12, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Houston, TX (United States)

Citations

IDCFRDescription
1472221 CFR 820.40Procedures not adequately established or maintained
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
315921 CFR 820.184DHR content