Stiriti Ayur Therapies Private Limited
FDA import alert and refusal historyHyderabad, IndiaFEI 2000027876
As of October 26, 2026, Stiriti Ayur Therapies Private Limited (Hyderabad, India) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for coleus forskolli extract; tribulus terrestris extract tt750 capsules with tribulosin, published by FDA on May 28, 2013, 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 Stiriti Ayur Therapies Private Limited
1 record, newest first. Each line links to the FDA page it came from.
2013
- Import alert listingListed on Import Alert 99-08red listColeus Forskolli Extract; Tribulus Terrestris Extract TT750 Capsules with TribulosinSource
Questions about Stiriti Ayur Therapies Private Limited
- Is Stiriti Ayur Therapies Private Limited on an FDA import alert?
- Yes. As of October 26, 2026, Stiriti Ayur Therapies Private Limited is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for coleus forskolli extract; tribulus terrestris extract tt750 capsules with tribulosin; FDA published the listing on May 28, 2013.
- Has FDA refused shipments from Stiriti Ayur Therapies Private Limited?
- No FDA import refusals for Stiriti Ayur Therapies Private Limited appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Stiriti Ayur Therapies Private Limited's FEI number?
- Stiriti Ayur Therapies Private Limited's FDA Establishment Identifier (FEI) is 2000027876.
- Can shipments from Stiriti Ayur Therapies Private Limited still enter the U.S.?
- Shipments of coleus forskolli extract; tribulus terrestris extract tt750 capsules with tribulosin from Stiriti Ayur Therapies Private Limited 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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