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Sea Pharm Co., LTD

FDA import alert and refusal historyPranakornsriayutthaya, ThailandFEI 3017140332

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Example subjectSea Pharm Co., LT added to Import Alert 16-129 (red list)

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As of October 26, 2026, Sea Pharm Co., LTD is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on August 19, 2020, most often for required label information not in english (NO ENGLISH).

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

Current status

Import alerts
Not listed
Last import refusal
Oral rehydration products · NO ENGLISH
Last warning letter
None found
Last inspection
None on record

Every FDA record for Sea Pharm Co., LTD

1 record, newest first. Each line links to the FDA page it came from.

2020

  1. Import refusal
    Refused, Oral rehydration productsNO ENGLISHEntry SCS-1113042-6
    Source

Refusal charges, in plain English

  • NO ENGLISH1 refused line

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

Questions about Sea Pharm Co., LTD

Is Sea Pharm Co., LTD on an FDA import alert?
No listing for Sea Pharm Co., LTD appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Thailand page.
Has FDA refused shipments from Sea Pharm Co., LTD?
Yes. FDA refused 1 shipment line from Sea Pharm Co., LTD on August 19, 2020. The most recent, on August 19, 2020, was oral rehydration products, charged as NO ENGLISH (required label information not in english).
Why did FDA refuse Sea Pharm Co., LTD's shipments?
The most frequent charge is NO ENGLISH (required label information not in english, 1 line).
What is Sea Pharm Co., LTD's FEI number?
Sea Pharm Co., LTD's FDA Establishment Identifier (FEI) is 3017140332.

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Example subjectSea Pharm Co., LT 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.