Drive DeVilbiss Healthcare LLC
Letter data
- Company
- Drive DeVilbiss Healthcare LLC
- Recipient
- Derek Lampert | Chief Executive Officer (CEO) | Drive DeVilbiss Healthcare LLC | 99 Seaview Blvd, Suite 210 | Port Washington | , | NY | 11050 | United States
- Issue date
- 2024-10-23
- Posted date
- Not available
- FDA office
- Office of Medical Device and Radiological Health Operations (Division 1)
- Subject
- Not available
- Product
- Medical Devices
- CMS ID
- 619182
- 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
Drive DeVilbiss Healthcare LLC
MARCS-CMS 619182 —
October 23, 2024
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About Warning and Close-Out Letters
Product:
Medical Devices
Recipient:
Recipient Name
Derek Lampert
Recipient Title
Chief Executive Officer (CEO)
Drive DeVilbiss Healthcare LLC
99 Seaview Blvd, Suite 210
Port Washington
,
NY
11050
United States
Issuing Office:
Office of Medical Device and Radiological Health Operations (Division 1)
United States
Secondary Issuing Offices
United States
Dear Mr. Lampert:
The Food and Drug Administration has completed an evaluation of your firm’s corrective actions in response to our Warning Letter CMS # 619182, dated November 23, 2021. Based on our evaluation, it appears that you have addressed the violation(s) 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.
Sincerely,
/S/
RDML Sean M. Boyd, MPH, USPHS
Director
Office of Regulatory Programs
Office of Product Evaluation and Quality
Center for Devices and Radiological Health
Content current as of:
10/30/2024
Regulated Product(s)
Medical Devices