Nutriloc Dried Foods Inc.
FDA import alert and refusal historyDelta, CanadaFEI 3005017268
As of October 26, 2026, Nutriloc Dried Foods Inc. (Delta, Canada) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for wolfberry (chinese or southeast asian berry of the chinese matrimony vine, w/slight licorice flavor); berries, n.e.c., published by FDA on October 2, 2009, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Nutriloc Dried Foods Inc.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-08red listWolfberry (Chinese or Southeast Asian berry of the Chinese matrimony vine, w/slight licorice flavor); Berries, N.E.C.Source
Questions about Nutriloc Dried Foods Inc.
- Is Nutriloc Dried Foods Inc. on an FDA import alert?
- Yes. As of October 26, 2026, Nutriloc Dried Foods Inc. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for wolfberry (chinese or southeast asian berry of the chinese matrimony vine, w/slight licorice flavor); berries, n.e.c.; FDA published the listing on October 2, 2009.
- Has FDA refused shipments from Nutriloc Dried Foods Inc.?
- No FDA import refusals for Nutriloc Dried Foods Inc. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Nutriloc Dried Foods Inc.'s FEI number?
- Nutriloc Dried Foods Inc.'s FDA Establishment Identifier (FEI) is 3005017268.
- Can shipments from Nutriloc Dried Foods Inc. still enter the U.S.?
- Shipments of wolfberry (chinese or southeast asian berry of the chinese matrimony vine, w/slight licorice flavor); berries, n.e.c. from Nutriloc Dried Foods Inc. can be detained without physical examination under Import Alert 99-08; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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