Lejal Lab Inc.
FDA import alert and refusal historyMeycauayan, PhilippinesFEI 3015214009
Recorded by FDA as LEJAL LAB INC.
As of October 25, 2026, Lejal Lab Inc. (Meycauayan, Philippines) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for liverguard silymarin lecithin capsules, published by FDA on March 12, 2020, 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 99-39 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Lejal Lab Inc.
1 record, newest first. Each line links to the FDA page it came from.
2020
- Import alert listingListed on Import Alert 99-39red listLiverGuard Silymarin Lecithin CapsulesSource
Questions about Lejal Lab Inc.
- Is Lejal Lab Inc. on an FDA import alert?
- Yes. As of October 25, 2026, Lejal Lab Inc. is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for liverguard silymarin lecithin capsules; FDA published the listing on March 12, 2020.
- Has FDA refused shipments from Lejal Lab Inc.?
- No FDA import refusals for Lejal Lab Inc. appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Lejal Lab Inc.'s FEI number?
- Lejal Lab Inc.'s FDA Establishment Identifier (FEI) is 3015214009.
- Can shipments from Lejal Lab Inc. still enter the U.S.?
- Shipments of liverguard silymarin lecithin capsules from Lejal Lab Inc. can be detained without physical examination under Import Alert 99-39; 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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