Granor Passi Langkloof (Pty) Ltd
FDA import alert and refusal historyLouterwater, South AfricaFEI 3004382446
As of October 26, 2026, Granor Passi Langkloof (Pty) Ltd has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on October 28, 2022, was classified VAI (Voluntary Action Indicated).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Granor Passi Langkloof (Pty) Ltd
2 records, newest first. Each line links to the FDA page it came from.
Questions about Granor Passi Langkloof (Pty) Ltd
- Is Granor Passi Langkloof (Pty) Ltd on an FDA import alert?
- No listing for Granor Passi Langkloof (Pty) Ltd appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the South Africa page.
- Has FDA refused shipments from Granor Passi Langkloof (Pty) Ltd?
- No FDA import refusals for Granor Passi Langkloof (Pty) Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Granor Passi Langkloof (Pty) Ltd last inspected by FDA?
- FDA's most recent inspection of Granor Passi Langkloof (Pty) Ltd with a final classification is dated October 28, 2022 and was classified VAI (Voluntary Action Indicated).
- What is Granor Passi Langkloof (Pty) Ltd's FEI number?
- Granor Passi Langkloof (Pty) Ltd's FDA Establishment Identifier (FEI) is 3004382446.
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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.