# Knoll LLC - Inspection Records

Source: https://www.globalkeysolutions.net/companies/knoll-llc/ebd1a68d-0882-4226-b98e-753e5cb87968

> Inspection records and compliance data for Knoll LLC in Jayuya, Puerto Rico. Access full analysis and detailed observations.

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## Details

- Name: Knoll LLC
- FEI Number: 2650166
- City: Jayuya
- State: Puerto Rico
- Country Name: United States
- Address Line 1: Road 144, Km 2.6
- Zip Code: 00664

## Related Documents

- [FDA Inspection 1080046 - Knoll LLC - 2019-02-12](https://www.globalkeysolutions.net/records/fda_inspections/knoll-llc/e5bc4f6e-a5c3-44de-82c6-805c0fc3d9f4) — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2019
- [FDA Inspection 1005493 - Knoll LLC - 2017-01-27](https://www.globalkeysolutions.net/records/fda_inspections/knoll-llc/ae16b6a0-8c2a-4c39-b403-6c4b5a5310b1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 27, 2017
- [FDA Inspection 947761 - Knoll LLC - 2015-10-23](https://www.globalkeysolutions.net/records/fda_inspections/knoll-llc/0b341280-ad1d-4563-8bd4-0791df982326) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 23, 2015
- [FDA Inspection 809680 - Knoll LLC - 2012-12-04](https://www.globalkeysolutions.net/records/fda_inspections/knoll-llc/401c73bd-604e-4c80-a1e6-01473622a415) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 4, 2012
- [FDA Inspection 734076 - Knoll LLC - 2011-07-12](https://www.globalkeysolutions.net/records/fda_inspections/knoll-llc/f1116876-40d2-4ebb-b50d-6e610422502c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 12, 2011
- [FDA Inspection 697044 - Knoll LLC - 2010-10-15](https://www.globalkeysolutions.net/records/fda_inspections/knoll-llc/091d49e6-96f3-4af4-ad71-1f7cbb17d6ad) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 15, 2010
- [FDA Inspection 589479 - Knoll LLC - 2009-06-12](https://www.globalkeysolutions.net/records/fda_inspections/knoll-llc/9b7a4f6a-0ff7-42d0-9113-85c89249af49) — classification: No Action Indicated (NAI), source: FDA, date: June 12, 2009

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