FDA Inspection 1232785 — SUPERSONIC IMAGINE

SUPERSONIC IMAGINE — FEI 3023269186

The FDA completed an inspection of SUPERSONIC IMAGINE on Mar 7, 2024 in Aix-En-Provence. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 7, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Aix-En-Provence (France)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
48621 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements