SupplierRadar

Pharma Sjrp

FDA import alert and refusal historySao Paulo, BrazilFEI 3043740628

Recorded by FDA as PHARMA SJRP

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Example subjectPharma Sjr added to Import Alert 16-129 (red list)

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As of October 26, 2026, Pharma Sjrp is not on any FDA import alert in SupplierRadar's records; FDA refused 5 of its shipment lines on May 5, 2026, 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
Protein n.e.c. · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Pharma Sjrp

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

2026

  1. Import refusal
    Refused, 5 lines in one entry: Protein n.e.c.; Nicotinamide (niacinamide) (vitamin) and 2 moreUNAPPROVEDEntry AEK-0351486-5Show 5 lines
    Source

Refusal charges, in plain English

  • UNAPPROVED5 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 Pharma Sjrp

Is Pharma Sjrp on an FDA import alert?
No listing for Pharma Sjrp appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Brazil page.
Has FDA refused shipments from Pharma Sjrp?
Yes. FDA refused 5 shipment lines from Pharma Sjrp on May 5, 2026. The most recent, on May 5, 2026, was protein n.e.c., charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Pharma Sjrp's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 5 lines).
What is Pharma Sjrp's FEI number?
Pharma Sjrp's FDA Establishment Identifier (FEI) is 3043740628.

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Example subjectPharma Sjr 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.