# K & M Citrus Inc., Weirsdale, FL – FDA Inspections

Source: https://www.keypedia.com/companies/k-m-citrus-inc/15dd5560-a1ff-4bec-9af2-6142f1fe8267

> Inspection records and compliance data for K & M Citrus Inc. in Weirsdale, Florida. 5 FDA inspections on record, last inspected May 01, 2024.

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## Details

- Name: K & M Citrus Inc.
- FEI Number: 3001452859
- Address Line 1: 16425 County Rd 42
- City: Weirsdale
- State: Florida
- Zip Code: 32195
- Country Name: United States
- Address: 16425 County Rd 42, Weirsdale, Florida 32195, United States
- Country: United States

## Related Documents

- FDA Inspection 1239133 - K & M Citrus Inc. - 2024-05-01 — classification: No Action Indicated (NAI), source: FDA, date: May 1, 2024
- FDA Inspection 1081396 - K & M Citrus Inc. - 2019-02-27 — classification: No Action Indicated (NAI), source: FDA, date: February 27, 2019
- FDA Inspection 966642 - K & M Citrus Inc. - 2016-03-03 — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2016
- FDA Inspection 966642 - K & M Citrus Inc. - 2016-03-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 3, 2016
- FDA Inspection 966642 - K & M Citrus Inc. - 2016-03-03 — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2016
- FDA Inspection 768518 - K & M Citrus Inc. - 2012-02-22 — classification: No Action Indicated (NAI), source: FDA, date: February 22, 2012
- FDA Inspection 768518 - K & M Citrus Inc. - 2012-02-22 — classification: No Action Indicated (NAI), source: FDA, date: February 22, 2012
- [FDA Inspection 768518 - K & M Citrus Inc. - 2012-02-22](https://www.keypedia.com/records/fda_inspections/k-m-citrus-inc/ff88d3fa-e7d5-428f-a3a3-935e3e954406) — classification: No Action Indicated (NAI), source: FDA, date: February 22, 2012
- FDA Inspection 736924 - K & M Citrus Inc. - 2011-09-06 — classification: No Action Indicated (NAI), source: FDA, date: September 6, 2011
- FDA Inspection 736924 - K & M Citrus Inc. - 2011-09-06 — classification: No Action Indicated (NAI), source: FDA, date: September 6, 2011

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