How many FDA warning letters has Umendra Life Sciences Private Limited received?

Argus HQ has recorded 1 FDA warning letter for Umendra Life Sciences Private Limited.

What FDA recalls has Umendra Life Sciences Private Limited issued?

Argus HQ has not recorded an FDA recall tied to Umendra Life Sciences Private Limited in our current dataset.

Is Umendra Life Sciences Private Limited 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 Umendra Life Sciences Private Limited. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

Umendra Life Sciences Private Limited

Name: FDA Enforcement Actions Against Umendra Life Sciences Private Limited
Creator: Argus HQ
License: https://argushq.ai/methodology

Industry: pharmaceutical

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 · cgmp2026-06-02
Umendra Life Sciences Private Limited — CGMP/OTC Finished Pharmaceuticals/Adulterated (2026-06-02)

Frequently asked questions

How many FDA warning letters has Umendra Life Sciences Private Limited received?: Argus HQ has recorded 1 FDA warning letter for Umendra Life Sciences Private Limited.
What FDA recalls has Umendra Life Sciences Private Limited issued?: Argus HQ has not recorded an FDA recall tied to Umendra Life Sciences Private Limited in our current dataset.
Is Umendra Life Sciences Private Limited 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 Umendra Life Sciences Private Limited. 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.