# Makoto Dressing, Inc., Melbourne, FL – FDA Inspections

Source: https://www.keypedia.com/companies/makoto-dressing-inc/01a31ad7-c196-4c43-83fa-df7ef16721e9

> Inspection records and compliance data for Makoto Dressing, Inc. in Melbourne, Florida. 4 FDA inspections on record, 1 Form 483, last inspected November 20, 2019.

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## Details

- Name: Makoto Dressing, Inc.
- FEI Number: 3004346772
- Address Line 1: 6922 Sonny Dale Dr
- City: Melbourne
- State: Florida
- Zip Code: 32904
- Country Name: United States
- Address: 6922 Sonny Dale Dr, Melbourne, Florida 32904, United States
- Country: United States

## Related Documents

- FDA Inspection 1113277 - Makoto Dressing, Inc. - 2019-11-20 — classification: No Action Indicated (NAI), source: FDA, date: November 20, 2019
- FDA Inspection 1113277 - Makoto Dressing, Inc. - 2019-11-20 — classification: No Action Indicated (NAI), source: FDA, date: November 20, 2019
- FDA Inspection 1051975 - Makoto Dressing, Inc. - 2018-05-07 — source: FDA, date: May 7, 2018
- [FDA Inspection 1006296 - Makoto Dressing, Inc. - 2017-03-23](https://www.keypedia.com/records/fda_inspections/makoto-dressing-inc/894749aa-030f-44a0-b6ec-92b3757006f5) — classification: No Action Indicated (NAI), source: FDA, date: March 23, 2017
- FDA Inspection 1006296 - Makoto Dressing, Inc. - 2017-03-23 — classification: No Action Indicated (NAI), source: FDA, date: March 23, 2017
- FDA Inspection 1006296 - Makoto Dressing, Inc. - 2017-03-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 23, 2017
- FDA Inspection 1006296 - Makoto Dressing, Inc. - 2017-03-23 — classification: No Action Indicated (NAI), source: FDA, date: March 23, 2017
- FDA Inspection 883345 - Makoto Dressing, Inc. - 2014-06-17 — classification: No Action Indicated (NAI), source: FDA, date: June 17, 2014
- FDA Inspection 883345 - Makoto Dressing, Inc. - 2014-06-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 17, 2014
- FDA Inspection 883345 - Makoto Dressing, Inc. - 2014-06-17 — classification: No Action Indicated (NAI), source: FDA, date: June 17, 2014

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