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Nestle Ghana Ltd

FDA import alert and refusal historyTema, GhanaFEI 3012864026

Recorded by FDA as NESTLE GHANA LTD

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Example subjectNestle Ghana Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Nestle Ghana Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on November 21, 2016, most often for lack notif (LACK NOTIF).

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

Current status

Import alerts
Not listed
Last import refusal
Instant cereal made with formula (baby) · LACK NOTIF
Last warning letter
None found
Last inspection
None on record

Every FDA record for Nestle Ghana Ltd

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

2016

  1. Import refusal
    Refused, Instant cereal made with formula (baby)LACK NOTIFNUTRIT LBLEntry K74-0185217-6
    Source

Refusal charges, in plain English

  • LACK NOTIF1 refused line

    LACK NOTIF

  • NUTRIT LBL1 refused line

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

Questions about Nestle Ghana Ltd

Is Nestle Ghana Ltd on an FDA import alert?
No listing for Nestle Ghana Ltd appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Ghana page.
Has FDA refused shipments from Nestle Ghana Ltd?
Yes. FDA refused 1 shipment line from Nestle Ghana Ltd on November 21, 2016. The most recent, on November 21, 2016, was instant cereal made with formula (baby), charged as LACK NOTIF (lack notif).
Why did FDA refuse Nestle Ghana Ltd's shipments?
The most frequent charges are LACK NOTIF (lack notif, 1 line) and NUTRIT LBL (nutrition information missing from label, 1 line).
What is Nestle Ghana Ltd's FEI number?
Nestle Ghana Ltd's FDA Establishment Identifier (FEI) is 3012864026.

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Example subjectNestle Ghana 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.