Extreme Xcience, Inc.
FDA import alert and refusal historyMetro Manila, PhilippinesFEI 3008993637
Recorded by FDA as EXTREME XCIENCE, INC.
As of October 26, 2026, Extreme Xcience, Inc. (Metro Manila, Philippines) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for greenlife veggie plus health drink, published by FDA on October 2, 2015, 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 Extreme Xcience, Inc.
1 record, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 99-39red listGreenlife Veggie Plus Health DrinkSource
Questions about Extreme Xcience, Inc.
- Is Extreme Xcience, Inc. on an FDA import alert?
- Yes. As of October 26, 2026, Extreme Xcience, Inc. is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for greenlife veggie plus health drink; FDA published the listing on October 2, 2015.
- Has FDA refused shipments from Extreme Xcience, Inc.?
- No FDA import refusals for Extreme Xcience, Inc. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Extreme Xcience, Inc.'s FEI number?
- Extreme Xcience, Inc.'s FDA Establishment Identifier (FEI) is 3008993637.
- Can shipments from Extreme Xcience, Inc. still enter the U.S.?
- Shipments of greenlife veggie plus health drink from Extreme Xcience, 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).
Buying from Extreme Xcience, Inc.?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.