FDA Warning Letter — ZIIP INC

Case 725870 — FEI 3029740697

The FDA took a Warning Letter action against ZIIP INC on May 22, 2026 (Pleasant Hill, CA). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
ZIIP INC
Date
May 22, 2026
Fiscal Year
2026
Product Type
Devices
Center
CDRH
Location
Pleasant Hill, CA (United States)