ZIIP INC

FDA inspection history in Pleasant Hill, California, 2026

1
Warning letter
1
Form 483

Every document, by year

  • Warning letter
  • Form 483

2026: one warning letter and one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2026One warning letter and one Form 483, at Pleasant Hill, California.

Cited most

Across all ZIIP observations on file

The complete ZIIP file.

All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$198

The price of the documents, added to your cart together

Sites

Documents

2 on file, newest first
DateDocumentPrice
2026-05-22Warning letter Warning letter$99
2026-01-12483 Form 483$99

Investigators on these documents

Sara M. Onyango (1)

FEI number 3029740697 · most recent document May 22, 2026

About ZIIP INC

How many FDA Form 483s has ZIIP INC received?

FDA Intel has 1 Form 483 on file for ZIIP INC; the most recent is dated Jan 12, 2026.

When was ZIIP INC last inspected by FDA?

The most recent FDA inspection document on file for ZIIP INC is a Form 483 dated Jan 12, 2026, for the site in Pleasant Hill, California.

What did FDA cite at ZIIP INC?

The regulations cited most in the observations on file for ZIIP INC are 21 CFR 820.30(f) (Design controls), 4 times; 21 CFR 803.50(a)(2) (If I am a manufacturer, what reporting requirements apply to me?), 1 time; 21 CFR 820.100(a) (Corrective and preventive action), 1 time.

Has ZIIP INC received an FDA warning letter?

Yes. FDA Intel has 1 FDA warning letter on file for ZIIP INC; the most recent is dated May 22, 2026.