# Creative Occasions, Inc., Nashville, TN – FDA Inspections

Source: https://www.keypedia.com/companies/creative-occasions-inc/c9c34e2c-5b59-4262-8eb3-dcb4ef88f086

> Inspection records and compliance data for Creative Occasions, Inc. in Nashville, Tennessee. 5 FDA inspections on record, 1 Form 483, last inspected April 13, 2017.

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## Details

- Name: Creative Occasions, Inc.
- FEI Number: 3004400914
- Address Line 1: 1605 County Hospital Rd
- City: Nashville
- State: Tennessee
- Zip Code: 37218
- Country Name: United States
- Address: 1605 County Hospital Rd, Nashville, Tennessee 37218, United States
- Country: United States

## Related Documents

- [FDA Inspection 1009051 - Creative Occasions, Inc. - 2017-04-13](https://www.keypedia.com/records/fda_inspections/creative-occasions-inc/49c81cda-371c-43eb-bc2d-6302deedb659) — source: FDA, date: April 13, 2017
- FDA Inspection 980912 - Creative Occasions, Inc. - 2016-08-03 — classification: No Action Indicated (NAI), source: FDA, date: August 3, 2016
- FDA Inspection 980912 - Creative Occasions, Inc. - 2016-08-03 — classification: No Action Indicated (NAI), source: FDA, date: August 3, 2016
- FDA Inspection 980912 - Creative Occasions, Inc. - 2016-08-03 — classification: No Action Indicated (NAI), source: FDA, date: August 3, 2016
- FDA Inspection 883375 - Creative Occasions, Inc. - 2014-06-11 — classification: No Action Indicated (NAI), source: FDA, date: June 11, 2014
- FDA Inspection 883375 - Creative Occasions, Inc. - 2014-06-11 — classification: No Action Indicated (NAI), source: FDA, date: June 11, 2014
- FDA Inspection 883375 - Creative Occasions, Inc. - 2014-06-11 — classification: No Action Indicated (NAI), source: FDA, date: June 11, 2014
- FDA Inspection 660875 - Creative Occasions, Inc. - 2010-05-05 — classification: No Action Indicated (NAI), source: FDA, date: May 5, 2010
- FDA Inspection 660875 - Creative Occasions, Inc. - 2010-05-05 — classification: No Action Indicated (NAI), source: FDA, date: May 5, 2010
- FDA Inspection 660875 - Creative Occasions, Inc. - 2010-05-05 — classification: No Action Indicated (NAI), source: FDA, date: May 5, 2010

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