Kevin J. Klug
Letter data
- Company
- Kevin J. Klug
- Recipient
- Kevin J. Klug | Owner | Kevin J. Klug | 56628 893rd Rd | Wynot | , | NE | 68792-3009 | United States
- Issue date
- 2020-03-12
- Posted date
- Not available
- FDA office
- Office of Human and Animal Food Division II West
- Subject
- Not available
- Product
- Not available
- CMS ID
- 588725
- 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
Kevin J. Klug
MARCS-CMS 588725 —
March 12, 2020
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Recipient:
Recipient Name
Kevin J. Klug
Recipient Title
Owner
Kevin J. Klug
56628 893rd Rd
Wynot
,
NE
68792-3009
United States
Issuing Office:
Office of Human and Animal Food Division II West
United States
913-495-5100
Dear Mr. Kevin J. Klug:
The Food and Drug Administration has completed an evaluation of Kevin J. Klug corrective actions in response to our Warning Letter (CMS case #: 588725) on September 23, 2019. 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/
Miguel A. Hernandez
Director, Compliance
Office of Human and Animal Food – Division II West
Content current as of:
03/18/2020