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Pokala Krishna

FDA import alert and refusal historyHyderabad, IndiaFEI 3018152987

Recorded by FDA as POKALA KRISHNA

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Example subjectPokala Krishn added to Import Alert 16-129 (red list)

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As of October 25, 2026, Pokala Krishna is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on April 13, 2021, most often for unapproved new drug (UNAPPROVED).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Herbals & botanicals (not teas), n.e.c. · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Pokala Krishna

2 records, newest first. Each line links to the FDA page it came from.

2021

  1. Import refusal
    Refused, 2 lines in one entry: Herbals & botanicals (not teas), n.e.c.UNAPPROVEDEntry SCS-4757788-9Show 2 lines
    Source

Refusal charges, in plain English

  • UNAPPROVED2 refused lines

    Unapproved new drug

    The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

Questions about Pokala Krishna

Is Pokala Krishna on an FDA import alert?
No listing for Pokala Krishna appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the India page.
Has FDA refused shipments from Pokala Krishna?
Yes. FDA refused 2 shipment lines from Pokala Krishna on April 13, 2021. The most recent, on April 13, 2021, was herbals & botanicals (not teas), n.e.c., charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Pokala Krishna's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
What is Pokala Krishna's FEI number?
Pokala Krishna's FDA Establishment Identifier (FEI) is 3018152987.

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Example subjectPokala Krishn added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.