Kratom Data 2022 (Food and Drug Administration)
Tracking # |
FDA22084435 |
Multi Request | Kratom Data 2022 |
Submitted | June 22, 2022 |
Est. Completion | None |
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Communications
From: Richard Baran
To Whom It May Concern:
Pursuant to the Freedom of Information Act, I hereby request the following records:
Any and all documents related to Mitragyna speciosa, kratom, Mitragynine and 7-hydroxymitragynine, or anything related to the previous plant.
Time frame requested 2012- current times
The requested documents will be made available to the general public, and this request is not being made for commercial purposes.
In the event that there are fees, I would be grateful if you would inform me of the total charges in advance of fulfilling my request. I would prefer the request filled electronically, by e-mail attachment if available or CD-ROM if not.
Thank you in advance for your anticipated cooperation in this matter. I look forward to receiving your response to this request within 20 business days, as the statute requires.
Sincerely,
Richard Baran
From: Food and Drug Administration
*** This is an automated message. Please do not reply to this email. ***
Reference: FDA22084435
Dear Requester,
This is to confirm that you submitted a request for record(s) from the Food and Drug Administration
pursuant to the Freedom of Information Act.
FOIA staff will review your request to determine whether it has sufficient information to be processed;
if so, you will receive another email as a formal acknowledgement of your request, with a control number for your request.
If your request is not sufficiently described,
or if there are any other deficiencies with your submission, FOIA staff will contact you via telephone or email.
From: Food and Drug Administration
Re: Confirmation # FDA22084435
The Food and Drug Administration (FDA) has received your Freedom of Information Act (FOIA) request for records regarding:
To Whom It May Concern: Pursuant to the Freedom of Information Act, I hereby request the following records: Any and all documents related to Mitragyna speciosa, kratom, Mitragynine and 7-hydroxymitragynine, or anything related to the previous plant. Time frame requested 2012- current times The requested documents will be made available to the general public, and this request is not being made for commercial purposes. In the event that there are fees, I would be grateful if you would inform me of the total charges in advance of fulfilling my request. I would prefer the request filled electronically, by e-mail attachment if available or CD-ROM if not. Thank you in advance for your anticipated cooperation in this matter. I look forward to receiving your response to this request within 20 business days, as the statute requires. Sincerely, Richard Baran Upload documents directly: https://www.muckrock.com/
The request has been declined for following reason: PLEASE RESUBMIT TO INDICATE THE TYPES OF RECORDS YOU ARE SEEKING SUCH AS APPROVAL RECORDS, ADVERSE EVENTS, INSPECTIONS, ETC. PLEASE ALSO SEE https://www.fda.gov/news-events/public-health-focus/fda-and-kratom FOR GENERAL INFORMATION. THANK YOU.
FOIA staff may contact you via telephone or E-mail. Note: Do NOT reply directly to this E-mail
From: Muckrock Staff
To Whom It May Concern:
I wanted to follow up on the following Freedom of Information Act request, copied below, and originally submitted on June 23, 2022. Please let me know when I can expect to receive a response. You had assigned it reference number #FDA22084435.
Thanks for your help, and let me know if further clarification is needed.
From: Muckrock Staff
To Whom It May Concern:
I wanted to follow up on the following Freedom of Information Act request, copied below, and originally submitted on June 23, 2022. Please let me know when I can expect to receive a response. You had assigned it reference number #FDA22084435.
Thanks for your help, and let me know if further clarification is needed.
From: Food and Drug Administration
Please provide your control number - It would start with 2022-. Thanks.
Sarah B. Kotler, J.D.
Director, Division of Freedom of Information
US FDA
301-796-8976
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