FDA Inspection 1247934 — Ceevra Inc.

Ceevra Inc. — FEI 3014132130

The FDA completed an inspection of Ceevra Inc. on Aug 26, 2024 in San Francisco, CA. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 26, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
San Francisco, CA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures