Fusion Autism Center | |
3662 Cedarcrest Rd Ste 220 Acworth GA 30101-8765 | |
(866) 610-0590 | |
Not Available |
Full Name | Fusion Autism Center |
---|---|
Speciality | Behavior Analyst |
Location | 3662 Cedarcrest Rd Ste 220, Acworth, Georgia |
Authorized Official Name and Position | Jason Owen (CEO) |
Authorized Official Contact | 4708166449 |
Accepts Medicare Insurance | This clinic does not participate in Medicare Program. |
Mailing Address | Practice Location Address |
---|---|
Fusion Autism Center 300 International Pkwy Ste 200 Lake Mary FL 32746-5028 Ph: (470) 816-6449 | Fusion Autism Center 3662 Cedarcrest Rd Ste 220 Acworth GA 30101-8765 Ph: (866) 610-0590 |
NPI Number | 1699322321 |
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Provider Enumeration Date | 08/19/2019 |
Last Update Date | 11/10/2022 |
Certification Date | 11/10/2022 |
Identifier | Type | State | Issuer |
---|---|---|---|
1699322321 | NPI | - | NPPES |
News Archive
The 2015 MacLean Center Prize in Clinical Ethics and Health Outcomes, a $50,000 award, will be presented to Laura Roberts, MD, MA, a graduate of the University of Chicago Pritzker School of Medicine, who is chair of the Department of Psychiatry and Behavioral Sciences at the Stanford University School of Medicine and an internationally recognized scholar in bioethics, psychiatry, medicine and medical education.
The health care world prepped for Hurricane Sandy by moving patients and shutting down offices.
As breast cancer awareness month is observed during October, the American Physical Therapy Association (APTA) is hoping to shine a spotlight on lymphedema, a chronic, debilitating and often irreversible side effect of cancer treatment.
The results of a study conducted in Brazil suggest that the sympathetic nervous system - the part of the autonomous nervous system that controls responses to danger or stress - can modulate the action of defense cells in patients with autoimmune diseases.
Guidant LLC pleaded guilty today in St. Paul, Minn., before U.S. District Court Judge Donovan W. Frank to criminal violations of the Federal Food, Drug and Cosmetic Act, the Justice Department announced. The medical device manufacturer's admission of criminal wrongdoing is the result of a four-year investigation into Guidant's handling of short-circuiting failures of three models of its implantable cardioverter defibrillators: the Ventak Prizm 2 DR (Model 1861) and the Contak Renewal (Models H135 and H155).
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