A.I.G Technologies, Inc.
Letter data
- Company
- A.I.G Technologies, Inc.
- Recipient
- Stephen Dawes | Technical Director | A.I.G Technologies, Inc. | 5001 NW 13th Avenue | Suite B | Deerfield Beach | , | FL | 33064 | United States
- Issue date
- 2020-02-18
- Posted date
- Not available
- FDA office
- Office of Pharmaceutical Quality Operations Division II
- Subject
- Not available
- Product
- Drugs
- CMS ID
- 490872
- Reference number
- Not available
- FEI
- Not available
- Inspection dates
- Not available
Normalized citations
21 CFR: None found
21 U.S.C.: None found
Related FDA links
No related FDA letter link is present in the source index.
Full source text
CLOSEOUT LETTER
A.I.G Technologies, Inc.
MARCS-CMS 490872 —
February 18, 2020
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Delivery Method:
VIA UPS
Product:
Drugs
Recipient:
Recipient Name
Stephen Dawes
Recipient Title
Technical Director
A.I.G Technologies, Inc.
5001 NW 13th Avenue
Suite B
Deerfield Beach
,
FL
33064
United States
Issuing Office:
Office of Pharmaceutical Quality Operations Division II
United States
Mr. Dawes,
The Food and Drug Administration has completed evaluation of your firm’s corrective actions in response to our Warning Letter [WL # 490872 dated December 5, 2017]. Based on our evaluation, it appears that you have addressed the violations contained in this Warning Letter. Future FDA inspections and regulatory activities will further assess the adequacy and sustainability of these corrections.
This letter does not relieve you or your firm from the responsibility of taking all necessary steps to assure sustained compliance with the Federal Food, Drug, and Cosmetic Act and its implementing regulations or with other relevant legal authority. The Agency expects you and your firm to maintain compliance and will continue to monitor your state of compliance. This letter will not preclude any future regulatory action should violations be observed during a subsequent inspection or through other means.
If you have questions regarding the contents of this letter, you may contact Jamillah Selby via phone at
215-490-8417
or email at
Jamillah.selby@fda.hhs.gov
.
Sincerely,
/S/
John W. Diehl, M.S
Director, Compliance Branch
Office of Pharmaceutical Quality Operations, Division II
Content current as of:
02/27/2020
Regulated Product(s)
Drugs