Inspections, Compliance, Enforcement, and Criminal Investigations
Johnson and Johnson Consumer Products, Inc. Close out Letter 11/23/10
Department of Health and Human Services
|Public Health Service
Food and Drug Administration
Telephone (973) 331-4906
November 23, 2010
Vice President, Global Regulatory Affairs
Johnson and Johnson Consumer Products, Inc.
199 Grandview Road
Skillman, New Jersey 08558
Dear Mr. Bowden:
The Food and Drug Administration has completed an evaluation of your firm's corrective actions in response to our Warning Letter Number 10-NWJ-17, dated September 27, 2010. 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.
Director, Compliance Branch
New Jersey District