Facility Graph → Food & Beverage → PETNET Solutions Inc

INDEXABLE (PASSES DATA-SUFFICIENCY GATE)

Food & Beverage FEI: 3011121261 🛡️ LEVEL 2 · VAI OBSERVATION FOLLOW-UP

PETNET Solutions Inc

Registered Address: Ohio, USA (USA)

For Brand Buyers: PETNET Solutions Inc carries a BBB (76/100) rating due to documented FDA activity centered on Incoming Ingredient Identity Testing & COA Qualification. Before wiring a deposit, require written proof of CAPA closure and third-party ISO 17025 finished-batch release testing.

Connected FDA Sources (1): FDA ORA FOIA Electronic Reading Room · Resolved Name Aliases: PETNET Solutions Inc

BBB

76/100

Moderate (VAI)

7-Dim FDA Record Index v2.0

Ranks in the 38th percentile among Food & Beverage facilities.

Based strictly on public U.S. FDA records as of 2026-11-03. See Formula v2.0

Dim 1 · Credit Grade

BBB (76/100)

Recency-Weighted Index

Dim 2 · Inspection Shield

Level 2 / 4

Physically Inspected — Documented Form 483 Observations

Dim 4 · 'Elsa' Audit Odds

81%

HIGH PRIORITY TARGET (Next 90–180 Days)

Dim 5 · 180d WL Escalation

49%

483 → Warning Letter Risk

Dim 6 · Brand Contagion

7 Brands

~35 Downstream SKUs

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LAYER 4 · AI BUYER DUE-DILIGENCE INTERVIEW SCRIPT Tailored to FEI 3011121261's FDA Record

5 Questions to Ask PETNET Solutions Inc Before Signing a Manufacturing Contract

Bring these exact questions to your discovery call with their QA Director or account rep before wiring a production deposit:

Q1: On 2026-02-17, FDA cited 21 CFR 111.153 (Incoming Ingredient Identity Testing & COA Qualification). Can your Quality Unit share the signed 15-day CAPA response and verification logs showing this gap is closed?
Q2: On 2026-02-17, FDA cited 21 CFR 120.24(a) (Electronic Record Data Integrity (21 CFR Part 11) & Retention). Can your Quality Unit share the signed 15-day CAPA response and verification logs showing this gap is closed?
Q3: Do you perform 100% FTIR/HPLC identity testing on incoming active ingredients in-house (21 CFR 111.75(a)(1)), or do you rely on vendor COAs?
Q4: Will you sign our Quality Agreement Rider requiring 24-hour notification if an FDA investigator issues a Form 482 or Form 483 at FEI 3011121261?
Q5: Can we review a redacted Master Manufacturing Record (MMR) and Batch Production Record (BPR) with dual-operator weight verification and yield reconciliation?

Cross-Database Regulatory & Inspection Timeline

Unified chronological history across FDA ORA Inspections, Form 483s, Warning Letters, Enforcement Recalls, and OASIS Import Refusals.

Form FDA 483 Issued · 2026-02-17

Open Full 483 Analysis & Dossier →

FDA Form 483 issued to PETNET Solutions Inc (FEI 3011121261) on 2026-02-17 following an inspection of its producer of regulated products operations in Ohio. The report documents 2 inspection observations centered on Incoming Ingredient Identity Testing & COA Qualification, Electronic Record Data Integrity (21 CFR Part 11) & Retention.

21 CFR 111.153 (Incoming Ingredient Identity Testing & COA Qualification): Failure to perform at least one test to verify the identity of every incoming dietary ingredient or raw component before use, or relying on a supplier's Certificate of Analysis (COA) without first qualifying the supplier.
21 CFR 120.24(a) (Electronic Record Data Integrity (21 CFR Part 11) & Retention): Uncontrolled spreadsheets, shared laboratory logins, missing audit trails, backdated entries, or failure to retain batch and distribution records for the statutory window. REPEAT OBSERVATION

Manufacturer Right-of-Reply & Free Match Correction

GUARDRAIL PROTECTED

To ensure fairness and accuracy, facility owners may submit verified Form 483 closeout evidence, CAPA completion statements, or entity-resolution corrections free of charge. Sponsorship never alters an FDA Record Index score.

Dimension 3 · FDA 6-System Model

6-Subsystem cGMP Radar Breakdown

Sub-scores mapped across FDA's six core inspection subsystems.

Quality System (CAPA & OOS) 65/100

Materials & Incoming Identity 69/100

Production & Batch Records 78/100

Facilities, Sanitation & Pest 80/100

Laboratory & Stability Controls 77/100

Packaging & Allergen Labeling 81/100

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