# Cospro Development Corporation, Reading, PA – FDA Inspections

Source: https://www.keypedia.com/companies/cospro-development-corporation/3405a404-c4eb-419f-9362-604c379f0347

> Inspection records and compliance data for Cospro Development Corporation in Reading, Pennsylvania. 4 FDA inspections on record, last inspected August 31, 2016.

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## Details

- Name: Cospro Development Corporation
- FEI Number: 3005123499
- Address Line 1: 101 N Front St
- City: Reading
- State: Pennsylvania
- Zip Code: 19601
- Country Name: United States
- Address: 101 N Front St, Reading, Pennsylvania 19601, United States
- Country: United States

## Related Documents

- [FDA Inspection 984991 - Cospro Development Corporation - 2016-08-31](https://www.keypedia.com/records/fda_inspections/cospro-development-corporation/add83829-8b73-4f9c-bc35-2851f7e84dfa) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 31, 2016
- FDA Inspection 984991 - Cospro Development Corporation - 2016-08-31 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 31, 2016
- FDA Inspection 791643 - Cospro Development Corporation - 2012-08-03 — classification: No Action Indicated (NAI), source: FDA, date: August 3, 2012
- [FDA Inspection 791643 - Cospro Development Corporation - 2012-08-03](https://www.keypedia.com/records/fda_inspections/cospro-development-corporation/ee57f928-ab0d-4bed-8310-e0c4df707b49) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 3, 2012
- FDA Inspection 733194 - Cospro Development Corporation - 2011-06-29 — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2011
- FDA Inspection 733194 - Cospro Development Corporation - 2011-06-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 29, 2011
- [FDA Inspection 635554 - Cospro Development Corporation - 2009-11-05](https://www.keypedia.com/records/fda_inspections/cospro-development-corporation/6cf67aaa-8fa3-4531-a199-2beff51201b8) — classification: No Action Indicated (NAI), source: FDA, date: November 5, 2009

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