Johnson & Johnson Consumer Inc FDA Inspection Record
Johnson & Johnson Consumer Inc is an FDA-inspected facility (FEI 2010632) located in Los Angeles, CA, US. RegDataLab tracks 4 FDA inspections at this facility.
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What FDA found at this site
- Latest inspection
- Mar 11, 2020: No Action Indicated (NAI)
- Inspections on record
- 4 (2 VAI, 2 NAI)
- Last OAI inspection
- None on record
- Warning letters
- None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
- Recalls as the recalling firm
- 1, latest Jan 5, 2011
- Import refusals
- 8
Inspections and what FDA cited
| Date | Result | What FDA cited |
|---|---|---|
| Mar 11, 2020 | No Action Indicated (NAI) | No citations listed |
| Oct 8, 2015 | Voluntary Action Indicated (VAI) | No citations listed |
| May 16, 2013 | No Action Indicated (NAI) | No citations listed |
| Aug 12, 2010 | Voluntary Action Indicated (VAI) | Quality control unit review of records (21 CFR 211.192) |
Recalls
| Date | Class | Recall | Product and reason |
|---|---|---|---|
| Jan 5, 2011 | Class III | F-0383-2011 | Rainbath Refreshing Shower and Bath Gel - Original, 40 oz, 360 units per pallet, Lot… The recall was initiated as a precautionary measure after routine testing conducted after the product lots were manufactured determined that… |
Facility details
- Company
- Johnson & Johnson Consumer Inc
- Location
- Los Angeles, CA (US)
- Source
- inspections