# Chartwell Pharmaceuticals Amityville, LLC - Inspection Records

Source: https://www.keypedia.com/companies/chartwell-pharmaceuticals-amityville-llc/d8360380-d99c-4c6b-a098-04d0bcc0f7c1

> Inspection records and compliance data for Chartwell Pharmaceuticals Amityville, LLC in Amityville, New York. Access full analysis and detailed observations.

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## Details

- Name: Chartwell Pharmaceuticals Amityville, LLC
- FEI Number: 2433247
- City: Amityville
- State: New York
- Country Name: United States
- Address Line 1: 369 Bayview Ave
- Zip Code: 11701
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, IN VITRO BIOEQUIVALENCE OR BIOANALYTICAL TESTING, PACK, REPACK

## Related Documents

- [483 - Chartwell Pharmaceuticals Amityville, LLC - 2022-12-21](https://www.keypedia.com/records/483/chartwell-pharmaceuticals-amityville-llc/726e0109-e40e-42ce-8c36-e43dd6c5ef08) — source: FDA, date: December 21, 2022
- [FDA Inspection 1193806 - Chartwell Pharmaceuticals Amityville, LLC - 2022-12-21](https://www.keypedia.com/records/fda_inspections/chartwell-pharmaceuticals-amityville-llc/16872dc1-e532-4f24-8636-36c17e46d0e3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 21, 2022
- [FDA Inspection 1193806 - Chartwell Pharmaceuticals Amityville, LLC - 2022-12-21](https://www.keypedia.com/records/fda_inspections/chartwell-pharmaceuticals-amityville-llc/835d60f1-5c38-4d3e-8413-2adfc3e91dcb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 21, 2022
- [483 - Chartwell Pharmaceuticals Amityville, LLC - 2019-02-13](https://www.keypedia.com/records/483/chartwell-pharmaceuticals-amityville-llc/d1cdf69f-9f0a-4fe6-94a0-1cbc864a8338) — source: FDA, date: February 13, 2019
- [FDA Inspection 1079804 - Chartwell Pharmaceuticals Amityville, LLC - 2019-02-13](https://www.keypedia.com/records/fda_inspections/chartwell-pharmaceuticals-amityville-llc/1c53ee15-e167-46c5-98e7-344d71a01d00) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 13, 2019
- [FDA Inspection 1011507 - Chartwell Pharmaceuticals Amityville, LLC - 2017-05-05](https://www.keypedia.com/records/fda_inspections/chartwell-pharmaceuticals-amityville-llc/62c85bc8-69bd-45a0-a590-99f38b6f85bd) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 5, 2017
- [FDA Inspection 980564 - Chartwell Pharmaceuticals Amityville, LLC - 2016-07-15](https://www.keypedia.com/records/fda_inspections/chartwell-pharmaceuticals-amityville-llc/ff7a3f71-f40d-4370-920b-b24092eaabd4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 15, 2016
- [FDA Inspection 935584 - Chartwell Pharmaceuticals Amityville, LLC - 2015-07-20](https://www.keypedia.com/records/fda_inspections/chartwell-pharmaceuticals-amityville-llc/0a358af1-6afb-4c29-b790-de0e14d3add5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 20, 2015
- [FDA Inspection 855253 - Chartwell Pharmaceuticals Amityville, LLC - 2013-10-30](https://www.keypedia.com/records/fda_inspections/chartwell-pharmaceuticals-amityville-llc/0df7424f-17b0-4688-964e-75ace27df1e5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 30, 2013
- [FDA Inspection 862838 - Chartwell Pharmaceuticals Amityville, LLC - 2013-10-30](https://www.keypedia.com/records/fda_inspections/chartwell-pharmaceuticals-amityville-llc/3e90ae43-775e-4fe1-9193-cc257c6798b0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 30, 2013
- [FDA Inspection 862838 - Chartwell Pharmaceuticals Amityville, LLC - 2013-10-30](https://www.keypedia.com/records/fda_inspections/chartwell-pharmaceuticals-amityville-llc/ea2b7ea8-3e08-4c00-92c6-cfb03f251e46) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 30, 2013
- [FDA Inspection 855253 - Chartwell Pharmaceuticals Amityville, LLC - 2013-10-30](https://www.keypedia.com/records/fda_inspections/chartwell-pharmaceuticals-amityville-llc/cc2cbf70-29c8-48df-98a0-7c95c7022707) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 30, 2013

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