FDA Letter API

CellEra LLC

Letter data

Company
CellEra LLC
Recipient
Richard E. Moon | Chief Financial Officer | CellEra LLC | 1045 Reed Dr, Ste C | Monroe | , | OH | 45050 | United States
Issue date
2022-07-21
Posted date
Not available
FDA office
Office of Medical Device and Radiological Health Division 1 – East
Subject
Not available
Product
Medical Devices
CMS ID
618209
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 CellEra LLC MARCS-CMS 618209 — July 21, 2022 More Warning Letters Warning Letters About Warning and Close-Out Letters Delivery Method: VIA UNITED PARCEL SERVICE Product: Medical Devices Recipient: Recipient Name Richard E. Moon Recipient Title Chief Financial Officer CellEra LLC 1045 Reed Dr, Ste C Monroe , OH 45050 United States Issuing Office: Office of Medical Device and Radiological Health Division 1 – East United States Dear Mr. Moon: The Food and Drug Administration has completed evaluation of your firm’s corrective actions in response to our Warning Letter, CMS# 618209, dated October 20, 2021 for your firm’s Monroe, OH location. 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/ Gina M. Brackett Director, Compliance Branch Office of Medical Devices & Radiological Health Division One - East Content current as of: 07/25/2022 Regulated Product(s) Medical Devices