Fitness Factory Group
FDA import alert and refusal historyLiverpool, United KingdomFEI 3013236331
Recorded by FDA as FITNESS FACTORY GROUP
As of October 26, 2026, Fitness Factory Group (Liverpool, United Kingdom) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for testaflex hormone augmentation; clomadex, published by FDA on April 7, 2017, 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 Fitness Factory Group
1 record, newest first. Each line links to the FDA page it came from.
2017
- Import alert listingListed on Import Alert 99-39red listTESTAFLEX Hormone Augmentation; ClomadexSource
Questions about Fitness Factory Group
- Is Fitness Factory Group on an FDA import alert?
- Yes. As of October 26, 2026, Fitness Factory Group is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for testaflex hormone augmentation; clomadex; FDA published the listing on April 7, 2017.
- Has FDA refused shipments from Fitness Factory Group?
- No FDA import refusals for Fitness Factory Group appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Fitness Factory Group's FEI number?
- Fitness Factory Group's FDA Establishment Identifier (FEI) is 3013236331.
- Can shipments from Fitness Factory Group still enter the U.S.?
- Shipments of testaflex hormone augmentation; clomadex from Fitness Factory Group 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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