Celex Laboratories Inc.
FDA import alert and refusal historyRichmond, CanadaFEI 3006525144
As of October 25, 2026, Celex Laboratories Inc. (Richmond, Canada) is on the red list of FDA Import Alert 54-14 (Supplements from firms not meeting supplement GMP) for vorst iron; vorst advanced join formula; vorst alpha lipoic acid, published by FDA on August 19, 2022, is also listed on Import Alert 99-39 (red list), and has 6 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 54-14 · red listIA 99-39 · red list
- Last import refusal
- Herbals & botanicals (not teas), n.e.c. · NCONTACT
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for Celex Laboratories Inc.
10 records, newest first. Each line links to the FDA page it came from.
2022
- Import alert listingListed on Import Alert 54-14red listVORST IRON; VORST Advanced Join Formula; Vorst Alpha Lipoic AcidSource
- Import alert listingListed on Import Alert 99-39red listVorst ironSource
- InspectionInspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2020
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and EconSource
2019
- Import refusalSource
Refused, 6 lines in one entry: Herbals & botanicals (not teas), n.e.c.; Animal by-products and extracts, n.e.c.NCONTACTFALSEEntry SCS-6172302-0Show 6 linesHide lines
- Refused, Herbals & botanicals (not teas), n.e.c.NCONTACTEntry SCS-6172302-0Source
- Refused, Herbals & botanicals (not teas), n.e.c.NCONTACTEntry SCS-6172302-0Source
- Refused, Herbals & botanicals (not teas), n.e.c.NCONTACTEntry SCS-6172302-0Source
- Refused, Animal by-products and extracts, n.e.c.FALSENCONTACTEntry SCS-6172302-0Source
- Refused, Herbals & botanicals (not teas), n.e.c.NCONTACTEntry SCS-6172302-0Source
- Refused, Herbals & botanicals (not teas), n.e.c.NCONTACTEntry SCS-6172302-0Source
Refusal charges, in plain English
- NCONTACT6 refused lines
No U.S. adverse event contact on supplement label
The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.
- FALSE1 refused line
False or misleading labeling
The labeling appeared to be false or misleading in some particular.
Questions about Celex Laboratories Inc.
- Is Celex Laboratories Inc. on an FDA import alert?
- Yes. As of October 25, 2026, Celex Laboratories Inc. is on the red list of FDA Import Alert 54-14, “Supplements from firms not meeting supplement GMP”, for vorst iron; vorst advanced join formula; vorst alpha lipoic acid; FDA published the listing on August 19, 2022.
- Has FDA refused shipments from Celex Laboratories Inc.?
- Yes. FDA refused 6 shipment lines from Celex Laboratories Inc. on September 13, 2019. The most recent, on September 13, 2019, was herbals & botanicals (not teas), n.e.c., charged as NCONTACT (no u.s. adverse event contact on supplement label).
- Why did FDA refuse Celex Laboratories Inc.'s shipments?
- The most frequent charges are NCONTACT (no u.s. adverse event contact on supplement label, 6 lines) and FALSE (false or misleading labeling, 1 line).
- When was Celex Laboratories Inc. last inspected by FDA?
- FDA's most recent inspection of Celex Laboratories Inc. with a final classification is dated February 25, 2022 and was classified OAI (Official Action Indicated).
- What is Celex Laboratories Inc.'s FEI number?
- Celex Laboratories Inc.'s FDA Establishment Identifier (FEI) is 3006525144.
- Can shipments from Celex Laboratories Inc. still enter the U.S.?
- Shipments of vorst iron; vorst advanced join formula; vorst alpha lipoic acid from Celex Laboratories Inc. can be detained without physical examination under Import Alert 54-14; 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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