FDA Inspection 1179170 — Meditherm Inc.

Meditherm Inc. — FEI 3006111110

The FDA completed an inspection of Meditherm Inc. on Sep 2, 2022 in Albuquerque, NM. 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
Sep 2, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Albuquerque, NM (United States)

Citations

IDCFRDescription
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
341521 CFR 820.22Quality Audit/Reaudit - conducted
366921 CFR 820.20(c)Management review - defined interval, sufficient frequency
48621 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements