How many FDA warning letters has ZIIP, Inc. received?

Argus HQ has recorded 1 FDA warning letter for ZIIP, Inc..

What FDA recalls has ZIIP, Inc. issued?

Argus HQ has not recorded an FDA recall tied to ZIIP, Inc. in our current dataset.

Is ZIIP, Inc. FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 1 warning letter, 0 recalls, and 0 approval records for ZIIP, Inc.. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

ZIIP, Inc.

Name: FDA Enforcement Actions Against ZIIP, Inc.
Creator: Argus HQ
License: https://argushq.ai/methodology

Industry: Medical Devices

Jurisdiction: US

FDA Warning Letter timeline

V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.

fda_warning_letter · cgmp2026-05-22
ZIIP, Inc. — CGMP/QSR/Medical Devices/Adulterated (2026-05-22)

Frequently asked questions

How many FDA warning letters has ZIIP, Inc. received?: Argus HQ has recorded 1 FDA warning letter for ZIIP, Inc..
What FDA recalls has ZIIP, Inc. issued?: Argus HQ has not recorded an FDA recall tied to ZIIP, Inc. in our current dataset.
Is ZIIP, Inc. FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 1 warning letter, 0 recalls, and 0 approval records for ZIIP, Inc.. Review the linked FDA source records directly before drawing a compliance conclusion.

Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.